Methods, Devices, Systems, and Kits for Automated Blood Collection by Fingerstick

ABSTRACT

Methods, devices, systems and kits for obtaining blood samples are provided. Devices include a cuff, a pressure source, and a timing mechanism. Devices may further include one or more of a: warming mechanism, lancing mechanism; automated sample collection device, automated sample analysis device, and communication unit. Systems include such a device, and may include sample collection, sample analysis, or communication devices. 
     Methods include placing a cuff on a digit of a subject, inflating the cuff, and obtaining a small volume blood sample. Methods may further include warming a digit; lancing a digit; pulsing the cuff; and providing a signal indicating the end of the sample collection time period. 
     Kits may include a device, a sample collection vessel, and may include a disposable for use in sample collection. 
     These methods, devices, systems and kits for obtaining blood samples may be used to easily, reliably, and consistently obtain blood samples from subjects.

BACKGROUND

Many clinical diagnostic methods require a blood sample from a subject.Blood samples include, for example, venous blood samples, arterial bloodsamples, capillary blood samples, and mixed venous blood samples.Obtaining a blood sample typically requires puncturing the skin of asubject. For example, arterial and venous blood samples are typicallyobtained by inserting a needle or catheter into an artery or vein inorder to obtain arterial or venous blood samples (respectively). Mixedvenous blood samples may be obtained from the pulmonary artery(requiring an invasive procedure). Arterial and venous blood samplesthus require puncturing the skin of a subject, in order to insert aportion of a needle or catheter into an artery or vein. Blood may beobtained without a needle, for example, by puncturing the skin of asubject and collecting blood that exits the puncture site. For example,a fingerstick blood sample may be obtained by lancing a digit (e.g., afinger) of a subject and collecting one or more drops of blood from thewound in the digit. Depending on the type and size of puncture, theamount of blood required, the time to obtain a blood sample, the qualityof blood samples may be variable.

However, many subjects find giving blood samples to be unpleasant andpainful. Moreover, different methods, different personnel (e.g.,phlebotomists), and different subjects may provide different amounts anddifferent qualities of blood when sampled. Thus, in addition to causingdiscomfort or pain to subjects, present methods of obtaining bloodsamples may be inconsistent, or may provide variable amounts of blood,or may provide blood samples of inadequate quality or integrity.Accordingly, improved methods of obtaining blood samples from subjectsare desired.

INCORPORATION BY REFERENCE

All publications, patents, and patent applications mentioned in thisspecification are herein incorporated by reference to the same extent asif each individual publication, patent, or patent application wasspecifically and individually indicated to be incorporated by reference.

COPYRIGHT

This document contains material subject to copyright protection. Thecopyright owner (Applicant herein) has no objection to facsimilereproduction of the patent documents and disclosures, as they appear inthe US Patent and Trademark Office patent file or records, but otherwisereserves all copyright rights whatsoever. The following notice shallapply: Copyright 2015 Theranos, Inc.

SUMMARY

Methods, devices, systems, and kits for obtaining blood samples fromsubjects are disclosed. In embodiments, devices, systems, methods, andkits disclosed herein are useful for collecting fingerstick bloodsamples from a digit (e.g., from a finger or toe). In embodiments, thesedevices, systems, methods, and kits provide automated pressure cyclingfor collection of blood during a fixed collection time period. Inembodiments, such automated pressure cycling is provided by aninflatable cuff which fits around a digit. Such a cuff may be inflatedand deflated repeatedly during at least part of the collection timeperiod. In embodiments, these devices, systems, methods, and kitsfurther provide digit warming as well as automated pressure cycling, andmay further provide digit lancing as well as automated pressure cyclingfor collection of blood during a fixed collection time period. Inembodiments, devices and systems as disclosed herein may include apressure-interruption switch. In embodiments, devices, systems, and kitsmay include a sample collection element or device; a communication unit;a sample analysis element or device; and combinations thereof.

These methods, devices, systems and kits for obtaining blood samples maybe used to easily and reliably obtain blood samples from subjects. Thesemethods, devices, systems, and kits are designed so that no extensiveamount of training or experience is required for their successful use inobtaining fingerstick samples from subjects. These methods, devices,systems, and kits provide advantages over previous methods, devices andsystems by, for example, reliably providing improved blood flow forfingerstick blood sample collection, providing accurate timing of suchsample collection, and greater ease of sample collection by a techniciancollecting a blood sample.

Small volume blood samples may be obtained from small punctures,incisions, or other wounds made in a digit of a subject (e.g., a fingeror toe) or other skin surface of a subject (e.g., of a heel, of anearlobe, or of another location). Small volume blood samples may beobtained from a digit of a subject within a short period of time afterthe puncture, incision, or other wound is made. In embodiments, a shortperiod of time is a time period which ends prior to the occurrence ofsignificant coagulation of a blood sample collected from an incision orwound in a digit. In embodiments, a short period of time is a timeperiod which ends prior to the occurrence of significant degradation ofthe integrity or of the quality of a blood sample collected from apuncture, an incision, or other wound in a digit. In embodiments, ashort period of time is a period of time during which blood flowing froma puncture, incision, or other wound in a digit is primarily capillaryblood, and such capillary blood is not significantly diluted by, orcontaminated with, interstitial fluid. In embodiments, a short period oftime is about 90 seconds or less, or is about 80 seconds or less, or isabout 70 seconds or less, or is about 60 seconds or less. Inembodiments, a short period of time is about 90 seconds. In embodiments,a short period of time is about 60 seconds.

Devices include a cuff configured to hold or encircle a digit and apressure source configured to inflate the cuff. In embodiments, such acuff is configured to compress or constrict at least a portion of adigit effective to reduce or curtail blood flow out of the digit. Inembodiments, such a cuff is configured to repeatedly compress orconstrict at least a portion of a digit (e.g., to repeatedly inflate anddeflate a cuff placed around a digit) effective to reduce or curtailblood flow out of the digit. In embodiments, devices include a cuff, apressure source, and a timing mechanism, wherein the cuff is operablyconnected to the pressure source, effective that the cuff may beinflated by the pressure source. A cuff may also be deflated followinginflation. In embodiments, the timing mechanism and the pressure sourceare operably connected so that the application of pressure to the cuffmay be regulated by the timing mechanism, effective that the cuff may beinflated for a desired period of time (termed a “pulse”); or may beinflated for a desired period of time and deflated for a desired periodof time; or may be repeatedly inflated for a desired period of time anddeflated for a desired period of time, providing a desired frequency ofinflation (i.e., a series of pulses provided at a pulse frequency).Devices may further include one or more of a: warming mechanism, lancingmechanism; sample collection mechanisms, which may be or include anautomated sample collection device; a sample analysis device, which maybe or include an automated sample analysis device; and communicationunit.

Thus, in embodiments, a device having features as disclosed herein mayinclude a cuff configured to hold or encircle a digit, a pressuresource, and a timing mechanism, wherein these elements are operablyconnected to inflate the cuff for a desired period of time, or torepeatedly inflate the cuff at a desired inflation frequency. Inembodiments, a timing mechanism of a device having features as disclosedherein may provide a signal, or may control a signal device effective toprovide a signal or multiple signals. In embodiments, such signals mayalert a user to an event, or indicate that an operation or procedure(e.g., lancing a digit) is to be performed, or that an operation orprocedure is to ended (e.g., end collecting a sample), or may indicatethe beginning of a period of time, or may indicate the end of a periodof time, or may signal other operation, event, or period of time. Inembodiments, a device having features as disclosed herein may include acuff configured to hold or encircle a digit, a pressure source, a timingmechanism, and a warming mechanism, wherein these elements are operablyconnected to warm the cuff (or to warm a digit within or in contact withthe cuff), and to inflate the cuff for a desired period of time, or torepeatedly inflate the cuff at a desired inflation frequency. Inembodiments, a device having features as disclosed herein may include acuff configured to hold or encircle a digit, a pressure source, and atiming mechanism, wherein these elements are operably connected toinflate the cuff for a desired period of time, or to repeatedly inflatethe cuff at a desired inflation frequency, the device also including alancing mechanism configured to lance an exposed portion of a digitdisposed within the cuff. In embodiments, a device having features asdisclosed herein may include a cuff configured to hold or encircle adigit, a pressure source, a timing mechanism, and a warming mechanism,wherein these elements are operably connected to warm the cuff (or towarm a digit within or in contact with the cuff), and to inflate thecuff for a desired period of time, or to repeatedly inflate the cuff ata desired inflation frequency (where each inflation is followed by adeflation of the cuff), the device also including a lancing mechanismconfigured to lance an exposed portion of a digit disposed within thecuff. In embodiments, devices and systems disclosed herein may include apressure-interruption switch configured to temporarily interruptinflation, or to temporarily allow deflation, of the cuff.

Systems include such a device (e.g., a device having a cuff, a pressuresource, and a timing mechanism; a device having a cuff, a pressuresource, a timing mechanism, and a warming mechanism; a device having acuff, a pressure source, a timing mechanism, and a lancing mechanism; ora device having a cuff, a pressure source, a timing mechanism, a warmingmechanism, and a lancing mechanism), and may include sample collection,sample analysis, or communication devices.

Methods include placing a cuff on a digit of a subject, inflating thecuff, and obtaining a small volume blood sample. Methods may furtherinclude warming a digit; lancing a digit; pulsing the cuff; andproviding a signal indicating the end of the sample collection timeperiod. Methods may also include temporarily interrupting inflation of acuff, for example, by activation of an interrupt switch to, e.g.,temporarily stop inflation, or to temporarily block a conduit betweenthe pressure source and the cuff, or to temporarily allow deflation ofthe cuff.

Kits may include a device, a sample collection vessel, and may include adisposable for use in sample collection.

Accordingly, Applicant discloses herein devices and systems including acuff, a source of pressure, and a timing mechanism, and optionally otherelements as discussed herein. Applicant discloses herein devices andsystems including a cuff, a source of pressure, and a timing mechanism,and including a warming mechanism configured to warm a digit. Applicantdiscloses herein devices and systems including a cuff, a source ofpressure, a timing mechanism, and including a lancing mechanismconfigured to puncture a digit effective to make a wound or incisionproviding blood for sample collection. Applicant discloses hereindevices and systems including a cuff, a source of pressure, a timingmechanism, and a sample collection mechanism, the sample collectionmechanism being configured to collect a small sample of blood from apuncture, incision, or other wound in a digit. Such devices may furtherinclude a lancing mechanism configured to puncture a digit effective tomake a wound or incision providing blood for sample collection.

Applicant discloses herein devices and systems including a cuff, asource of pressure, a timing mechanism, and including an automatedsample analysis device or an automated sample analysis system. Applicantdiscloses herein devices and systems including a cuff, a source ofpressure, a timing mechanism, and including a communication uniteffective to transmit data regarding a blood sample. Applicant disclosesherein devices and systems including a cuff, a source of pressure, atiming mechanism, an automated sample analysis device or an automatedsample analysis system, and including a communication unit effective totransmit data regarding a blood sample.

Applicant discloses herein devices and systems including a cuff, asource of pressure, a means to pulse the application of pressure, and atiming mechanism. As used herein, to pulse the application of pressurerefers to periodic application of pressure, where periods of pressureapplication are separated by periods of release of pressure. Forexample, where pressure is applied to a digit by a cuff placed aroundthe digit, a pulse of pressure is provided by inflation of the cuff, andrepeated pulses are provided by repeated inflations of the cuffseparated by (at least partial) deflations of the cuff. Repeated pulsesof pressure (cycles of pressure), e.g., repeated pulses of inflation(cycles of inflation) may be provided at a desired frequency, where thefrequency is determined by the time between inflations.

Applicant discloses herein devices and systems including a cuff, asource of pressure, a means to pulse the application of pressure, atiming mechanism, and including a warming mechanism configured to warm adigit. Applicant discloses herein devices and systems including a cuff,a source of pressure, a means to pulse the application of pressure, atiming mechanism, and further including a lancing mechanism configuredto puncture a digit effective to make a wound or incision providingblood for sample collection, and optionally including a warmingmechanism configured to warm a digit. Applicant discloses herein devicesand systems including a cuff, a source of pressure, a means to pulse theapplication of pressure, a timing mechanism, and a sample collectionmechanism for collecting a small sample of blood, and optionallyincluding a warming mechanism configured to warm a digit. Applicantdiscloses herein devices and systems including a cuff, a source ofpressure, a means to pulse the application of pressure, a timingmechanism, a lancing mechanism configured to puncture a digit effectiveto make a wound or incision providing blood for sample collection, asample collection mechanism for collecting a small sample of blood, andoptionally including a warming mechanism configured to warm a digit. Awarming mechanism may be a variable warming mechanism, configured toprovide greater or lesser amounts of warming, i.e., may be configured towarm a digit to different temperatures. A variable warming mechanism maybe configured to warm a digit to a desired temperature. For example, avariable warming mechanism may be configured to warm a digit to about 2°C. above normal skin temperature, or to about 3° C. above normal skintemperature, or to about 4° C. above normal skin temperature, or toabout 5° C. above normal skin temperature, or higher

Applicant discloses herein devices and systems including a cuff, asource of pressure, a timing mechanism, and including an automatedsample analysis device or an automated sample analysis system. Applicantdiscloses herein devices and systems including a cuff, a source ofpressure, a timing mechanism, and including a communication uniteffective to transmit data regarding a blood sample. Applicant disclosesherein devices and systems including a cuff, a source of pressure, atiming mechanism, an automated sample analysis device or an automatedsample analysis system and including a communication unit effective totransmit data regarding a blood sample.

The methods, devices, and systems disclosed herein may be used to obtainblood samples from subjects. Blood samples may be obtained from a digitof a subject, e.g., from a finger or a toe of a subject, or other skinsurface. The methods, devices, and systems disclosed herein may be usedto obtain blood samples for clinical use, including, for example, forscreening, monitoring, diagnostic, research, and other uses.

In embodiments, the devices, systems, methods, and kits are configuredto aid in the collection of blood from puncture, incision, or otherwound in a digit or other skin surface of a subject. In embodiments,aiding the collection of blood from a puncture, incision or other woundincludes increasing the flow of blood from the wound for samplecollection (as compared to the flow that would otherwise occur). Inembodiments, such collection of blood is aided by inflation of a cuffeffective to compress or constrict at least a portion of a digit and soto reduce or curtail blood flow out of the digit.

In embodiments, the devices and systems disclosed herein are configuredto apply pressure to a digit to aid in collecting blood from a punctureor incision in that digit. In embodiments, the devices and systemsdisclosed herein are configured to apply pressure pulses to a digit toaid in collecting blood from a puncture or incision in that digit. Inembodiments, the devices and systems disclosed herein are configured toapply pressure pulses for a period of time to a digit to aid incollecting blood from a puncture or incision in that digit. Inembodiments, the period of time is determined by a timing mechanism; inembodiments, such a timing mechanism is included in the devices andsystems disclosed herein. In embodiments, the devices and systemsdisclosed herein are configured to apply pressure pulses to a digit toaid in collecting blood from a puncture or incision in that digit, wheresuch pressure pulses are applied at a desired frequency. In embodiments,the devices and systems disclosed herein are configured to applypressure pulses to a digit to aid in collecting blood from a puncture orincision in that digit, where such pressure pulses are separated by oneor more periods of lesser pressure, or of no pressure. In embodiments,the devices and systems disclosed herein are configured to applypressure pulses to a digit to aid in collecting blood from a puncture orincision in that digit, where such pressure pulses are provided at adesired frequency and such pulses are separated by one or more periodsof lesser pressure, or of no pressure. Such periods of applied pressuremay be set to be of a desired duration, and such periods of lesser or nopressure may be set to be of a desired duration.

In embodiments, the devices and systems disclosed herein are configuredto apply pressure to a digit to aid in collecting blood from a punctureor incision in that digit, and to warm at least a portion of that digit.In embodiments, such warming precedes collection of blood from thatdigit. In embodiments, the devices and systems disclosed herein areconfigured to apply pressure to a digit to aid in collecting blood froma puncture or incision in that digit, and include an element configuredto puncture, or to otherwise wound, a digit of a subject effective toprovide a passage for the flow of that subject's blood out of thatdigit.

In embodiments of the methods disclosed herein, a digit of a subject iscompressed by a cuff of a device or system disclosed herein, and is thenpunctured, or otherwise wounded, effective to provide a passage for theflow of that subject's blood out of that digit. In embodiments of themethods disclosed herein, a digit of a subject is warmed and iscompressed by a cuff of a device or system disclosed herein, and is thenpunctured, or otherwise wounded, effective to provide a passage for theflow of that subject's blood out of that digit. In embodiments of suchmethods, such warming precedes lancing of the digit, and precedescollection of blood from that digit. In embodiments, a digit is warmedfor at least about 30 seconds, or at least about 45 seconds, or at leastabout 60 seconds prior to lancing of the digit. Warming of a digit maybe provided by a cuff applied to the digit; in embodiments, warmingprecedes inflation of the cuff. In embodiments, warming may be providedwhile the cuff is inflated. In embodiments, warming may be providedprior to inflation of the cuff, and also while the cuff is inflated.

In embodiments of such methods disclosed herein, wherein a digit of asubject is compressed by a cuff of a device or system disclosed herein,such compression may comprise application of pressure for a period oftime to a digit to aid in collecting blood from a puncture or incisionin that digit. In embodiments, the period of time may be determined by atiming mechanism; in embodiments, the period of time may be determinedby an operator of the device or system. In embodiments, the period oftime is a short period of time. In embodiments, the period of time maybe a period of time which ends prior to the occurrence of significantcoagulation of a blood sample collected from an incision or wound in adigit. In embodiments, the period of time is a period which ends priorto the occurrence of significant degradation of the integrity or of thequality of a blood sample collected from an incision or wound in adigit. In embodiments, the period of time is a period which ends priorto significant mixing of interstitial fluid with blood in a samplecollected from an incision or wound in a digit.

In embodiments of such methods disclosed herein, wherein a digit of asubject is compressed by a cuff of a device or system disclosed herein,such compression may comprise pulses of pressure applied to that digit.In embodiments of such methods disclosed herein comprising pulses ofpressure, such pressure pulses may be applied at a desired frequency. Inembodiments, such pressure pulses may be separated by one or moreperiods of lesser pressure, or of no pressure. In embodiments, suchpressure pulses may be provided at a desired frequency and such pulsesare separated by one or more periods of lesser pressure, or of nopressure, where such periods are of a desired duration.

In embodiments of the methods disclosed herein, a digit of a subject maybe punctured, or otherwise wounded, by manual lancing effective toprovide a passage for the flow of that subject's blood out of thatdigit. In embodiments of the methods disclosed herein, a digit of asubject is compressed by a cuff of a device or system disclosed herein,and is then punctured, or otherwise wounded, by manual lancing effectiveto provide a passage for the flow of that subject's blood out of thatdigit. In embodiments of the methods disclosed herein, a digit of asubject is warmed and is compressed by a cuff of a device or systemdisclosed herein, and is then punctured, or otherwise wounded, by manuallancing effective to provide a passage for the flow of that subject'sblood out of that digit.

In embodiments of the methods disclosed herein, a digit of a subject maybe punctured, or otherwise wounded, effective to provide a passage forthe flow of that subject's blood out of that digit, by a device orsystem disclosed herein. In embodiments of the methods disclosed herein,a digit of a subject is compressed by a cuff of a device or systemdisclosed herein, and is then punctured, or otherwise wounded, by adevice or system disclosed herein effective to provide a passage for theflow of that subject's blood out of that digit. In embodiments of themethods disclosed herein, a digit of a subject is warmed and iscompressed by a cuff of a device or system disclosed herein, and is thenpunctured, or otherwise wounded, by a device or system disclosed hereineffective to provide a passage for the flow of that subject's blood outof that digit.

Applicant further provides a kit for fingerstick blood collection,comprising a device as disclosed herein and a sample collection vessel.In an embodiment, a kit for fingerstick blood collection comprises adevice as disclosed herein, a sample collection vessel, and a disposablefor use in sample collection. In embodiments, a disposable for use insample collection may be a sterile swab (e.g., an alcohol swab), may bean absorbent pad (e.g., a cotton gauze pad for placement over afingerstick wound), may be a bandage (e.g., a small self-adhesivebandage for placement over a fingerstick wound or over a gauze pad on afingerstick wound), other disposables for use in a sample collectionlocation (e.g., a clinical laboratory, a doctor's office, a clinic, aretail location, or other location in which a fingerstick sample may beobtained from a subject), and combinations thereof. In embodiments, asample may be collected at a point-of-care location, such as apoint-of-care location selected from the group of point-of-carelocations consisting of a hospital, a doctor's office, a clinic, andcombinations thereof.

On occasion, according to prior methods, a finger of a subject may havebeen manually squeezed by a technician prior to, or during, collectionof a fingerstick blood sample. However, the amount and duration ofsqueezing may have varied depending on the phlebotomist obtaining thefingerstick sample and the subject from whom it is obtained, thusleading to undesirable variation in the amount and quality of bloodobtained from a fingerstick.

The devices, systems, and methods disclosed herein provide advantagesover prior methods by automating some or all steps required for thecollection of fingerstick blood samples from a subject. In priormethods, a technician gripped a digit and applied pressure to the digitmanually. In embodiments, the devices, systems, and methods disclosedherein provide automation of some or all steps required for thecollection of fingerstick blood samples from a subject. Thus, thedevices, systems, and methods disclosed herein provide an advantage byeliminating the dependency on technician grip technique by applyingpressure to a digit by inflating a cuff placed around the digit. Thus,the devices, systems, and methods disclosed herein comprising aninflatable cuff improve methods for obtaining small blood samples byminimizing the amount of technician training that is required to train atechnician to extract a quality blood sample from a fingerstick. Thedevices, systems, and methods disclosed herein provide advantages byproviding control of the total time allowed for fingerstick bloodcollection. The devices, systems, and methods disclosed herein provideadvantages by improving standardization and consistency of thefingerstick blood collection process. The devices, systems, and methodsdisclosed herein provide advantages by providing a signal indicating thebeginning of a time period for blood collection. The devices, systems,and methods disclosed herein provide advantages by providing a signalindicating the end of an optimal time period for blood collection. Thedevices, systems, and methods disclosed herein provide advantages bypreventing blood collection at times outside of the optimal time periodfor fingerstick blood collection. By automating some or all steps of thefingerstick blood collection process, the devices, systems, and methodsdisclosed herein provide advantages by reducing or eliminating thepotential for repetitive motion injury of the phlebotomists' hands.

Applicant discloses herein methods, devices, systems, and kits forautomated fingerstick blood collection. These methods, devices, systems,and kits are simple and straight-forward to use. These methods, devices,systems, and kits are designed so that no extensive amount of trainingor experience is required for their successful use in obtainingfingerstick samples from subjects. Thus, the methods, devices, systems,and kits disclosed herein are designed for use by both sophisticated andunsophisticated technicians and phlebotomists, and offer advantagesincluding ease of use and wide applicability. The advantages provided bythe methods, devices and systems disclosed herein include, for example,improved blood flow for fingerstick blood sample collection, moreaccurate timing of such sample collection, greater control over thequality of the blood sample collected by avoidance of over-longcollection periods (which may result in excessive contamination of theblood sample by interstitial fluid), and greater ease of samplecollection by a technician. The advantages provided by the methods,devices and systems disclosed herein further include, for example,greater control and greater consistency of sample collection, andreduced risk of unsuccessful sample collection.

This Summary is provided to introduce a selection of concepts in asimplified form that are further described below in the DetailedDescription. This Summary is not intended to identify key features oressential features of the claimed subject matter, nor is it intended tobe used to limit the scope of the claimed subject matter.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows an exemplary device having features as disclosed herein,including a pressure cuff attached to a control unit, the control unitincluding a pump effective to apply pressure to the cuff under thecontrol of the control unit, and a power cable for connecting to a powersource (e.g., an electrical cable with plug for connecting to anelectrical power outlet).

FIG. 2A is a schematic diagram showing elements of an exemplary deviceas disclosed herein, including a housing with an ON/OFF switch andcontaining a pressure source connected to a cuff configured to constricta digit, a timer, a signal source, a power supply connected to a powercable, and a link to an (optional) foot pedal (interrupt switch).

FIG. 2B is a schematic diagram showing elements of an exemplary deviceas disclosed herein, including a housing with an ON/OFF switch andcontaining a pressure source connected to a cuff configured to constricta digit, the cuff including a warming element, a timer, a signal source,a power supply connected to a power cable, and an (optional) link to afoot pedal (interrupt switch). In embodiments, such a device may furtherinclude a sample collection device (not shown).

FIG. 2C is a schematic diagram showing elements of an exemplary deviceas disclosed herein, including a housing with an ON/OFF switch andcontaining a pressure source connected to a cuff configured to constricta digit, the device including a lancing device, a timer, a signalsource, a power supply connected to a power cable, and an (optional)link to a foot pedal (interrupt switch). In embodiments, the cuff mayinclude a warming element (not shown in the figure).

FIG. 2D is a schematic diagram showing elements of an exemplary deviceas disclosed herein, including a housing with an ON/OFF switch andcontaining a pressure source connected to a cuff configured to constricta digit, a timer, a signal source, a power supply connected to a powercable, a communication element, and an (optional) link to a foot pedal(interrupt switch). In embodiments, the cuff may include a warmingelement (not shown in the figure).

FIG. 2E is a schematic diagram showing elements of an exemplary deviceas disclosed herein, including a housing with an ON/OFF switch andcontaining a pressure source connected to a cuff configured to constricta digit, a timer, a signal source, a lancing device, a sample collectionelement, a power supply connected to a power cable, and an (optional)link to a foot pedal (interrupt switch). In embodiments, the cuff mayinclude a warming element (not shown in the figure).

FIG. 3A is a schematic diagram showing elements of an exemplary systemincluding a device as shown in FIGS. 1 and 2A-2E, including a housingwith an ON/OFF switch and containing a pressure source connected to acuff configured to constrict a digit, a timer, a signal source, a samplecollection element, a power supply connected to a power cable, and an(optional) link to a foot pedal (interrupt switch). In embodiments, thecuff may include a warming element (not shown in the figure). Inaddition to the device within and associated with the housing, thesystem includes an automated sample analysis device.

FIG. 3B is a schematic diagram showing elements of an exemplary systemincluding a device as disclosed herein, the device including a housingwith an ON/OFF switch and containing a pressure source connected to acuff configured to constrict a digit, a timer, a signal source, alancing device, a sample collection element, a power supply connected toa power cable, and an (optional) link to a foot pedal (interruptswitch). In embodiments, the cuff may include a warming element (notshown in the figure). In addition to the device within and associatedwith the housing, the system includes an automated sample analysisdevice.

FIG. 4A is a schematic diagram showing methods which may be performedusing the devices and systems disclosed herein, effective to automatemuch of the process of obtaining blood from a subject by fingerstick.Blood may be collected by fingerstick following application of pressureto a digit via a cuff placed around a digit, and lancing of the digit.In embodiments, a digit may be warmed prior to lancing. In embodiments,blood may be collected by manual fingerstick; for example, lancing maybe manually performed, blood collection may be manually collected, orboth lancing and collection may be performed manually. In embodiments,lancing may be automatically performed, blood collection may beautomatically collected, or both lancing and collection may be performedautomatically. The horizontal line beginning above the “Inflate Cuff”step and ending above the “Signal End” step indicates the time periodduring which the cuff is inflated; the dashed portion of that lineindicates that (optionally) the cuff may be deflated before thecollection period has ended (i.e., while collection continues).

FIG. 4B is a schematic diagram showing methods which may be performedusing the devices and systems disclosed herein, effective to automatemuch of the process of obtaining blood from a subject by fingerstick.Blood may be collected by fingerstick following application of pressureto a digit via a cuff placed around a digit, lancing of the digit, andpulsing the pressure applied by the cuff. In embodiments, blood may becollected by manual fingerstick; for example, lancing may be manuallyperformed, blood collection may be manually collected, or both lancingand collection may be performed manually. In embodiments, lancing may beautomatically performed, blood collection may be automaticallycollected, or both lancing and collection may be performedautomatically. The horizontal line beginning above the “Inflate Cuff”step and ending above the “Signal End” step indicates the time periodduring which the cuff is inflated; the diagonal lines indicate the timeperiod during which pulses of inflation may be applied (during which thecuff is repeatedly inflated and at least partially deflated betweenperiods of inflation). Such pulsing may begin at any suitable time aftercollection of blood has begun, and may begin at the same time as bloodcollection is begun.

FIG. 4C is a schematic diagram showing methods which may be performedusing the devices and systems disclosed herein, effective to automatemuch of the process of obtaining blood from a subject by fingerstick. Adigit may be warmed, and blood may be collected by fingerstick followingapplication of pressure to a digit via a cuff placed around a digit,lancing of the digit, with pulsing the pressure applied by the cuff. Thehorizontal line beginning above the “Inflate Cuff” step and ending abovethe “Signal End” step indicates the time period during which the cuff isinflated; the diagonal lines indicate the time period during whichpulses of inflation may be applied (during which the cuff is repeatedlyinflated and at least partially deflated between periods of inflation).Such pulsing may begin at any suitable time after collection of bloodhas begun, and may begin at the same time as blood collection is begun.

FIG. 4D is a schematic diagram showing methods which may be performedusing the devices and systems disclosed herein, effective to automatemuch of the process of obtaining blood from a subject by fingerstick.Blood may be collected by fingerstick following application of pressureto a digit via a cuff placed around a digit, warming the digit, lancingof the digit, with pulsing the pressure applied by the cuff. Warming maybe provided by a cuff having a warming element, for example, as shown inFIG. 2B. The horizontal line beginning above the “Inflate Cuff” step andending above the “Signal End” step indicates the time period duringwhich the cuff is inflated; the diagonal lines indicate the time periodduring which pulses of inflation may be applied (during which the cuffis repeatedly inflated and at least partially deflated between periodsof inflation). Such pulsing may begin at any suitable time aftercollection of blood has begun, and may begin at the same time as bloodcollection is begun.

FIG. 5 shows housings and portions of a conduit and a power connectionof devices having features as disclosed herein, providing examples ofdevices in three possible configurations. Individual configurations areindicated by illumination of indicator lights. The left-most indicatorlight of the device depicted on the left of the figure is shownilluminated to indicate that pressure is being applied by the device toa finger of a subject. The central indicator light of the devicedepicted in the middle of the figure is shown illuminated to indicatethat a lancet is to be applied to a finger of a subject to provide afingerstick wound for obtaining blood from the subject. The right-mostindicator light of the device depicted on the right of the figure isshown illuminated to indicate that blood may be collected from thefingerstick wound of the finger of the subject.

FIG. 6 shows housings and portions of conduits and power connections ofdevices having features as disclosed herein, providing examples ofdevices with error indicator lights lit in each of two configurations.Individual configurations are indicated by illumination of indicatorlights. The left error indicator light of the device depicted on thedevice on the left portion of the figure is shown illuminated toindicate that an error condition has occurred related to the pressurecuff. The right error indicator light of the device depicted on theright portion of the figure is shown illuminated to indicate that anerror condition has occurred related to the foot pedal (which is used tointerrupt the sequence of pressure pulses in the cuff).

FIG. 7A provides a schematic diagram detailing steps of obtaining afingerstick blood sample according to methods of using the devices andsystems disclosed herein. The figure explicitly names the digit as afinger, although a fingerstick blood sample may be obtained from a toe,or other body surface.

FIG. 7B provides a schematic diagram detailing steps of obtaining afingerstick blood sample according to methods of using the devices andsystems disclosed herein, in which a digit (e.g., a finger) is warmedprior to placing a cuff on the digit.

DETAILED DESCRIPTION

Description and disclosure of examples of methods, devices, and systemswhich may use, or be used with, method, devices, and systems disclosedherein may be found, for example, in U.S. Patent Application 61/874,893,filed Sep. 6, 2013; U.S. Patent Application 61/803,449, filed Mar. 19,2013; U.S. patent application Ser. No. 14/220,013, filed Mar. 19, 2014;in U.S. patent application Ser. No. 14/183,503, filed Feb. 18, 2014; inU.S. Pat. No. 8,840,838, filed Sep. 26, 2011; in U.S. Pat. No.8,475,739, filed Sep. 26, 2011; and in U.S. Pat. No. 8,435,738, filedSep. 26, 2011, the disclosures of which patents and patent applicationsare all hereby incorporated by reference in their entireties.

DEFINITIONS

Before the present methods, devices, and systems are disclosed anddescribed, it is to be understood that the terminology used herein isfor the purpose of describing particular embodiments only and is notintended to be limiting. It is also to be understood that the presentdisclosure provides explanatory and exemplary descriptions and examples,so that, unless otherwise indicated, the devices, systems, and methodsdisclosed herein are not limited to the specific embodiments describedherein. Accordingly, in this specification and in the claims whichfollow, reference will be made to a number of terms which shall bedefined to have the following meanings:

“Optional” or “optionally” means that the subsequently describedcircumstance may or may not occur, so that the description includesinstances where the circumstance occurs and instances where it does not.For example, if a device optionally contains a feature for a samplecollection unit, this means that the sample collection unit may or maynot be present, and, thus, the description includes both structureswherein a device possesses the sample collection unit and structureswherein sample collection unit is not present.

As used herein, the terms “substantial” means more than a minimal orinsignificant amount; and “substantially” means more than a minimally orinsignificantly. Thus, for example, the phrase “substantiallydifferent”, as used herein, denotes a sufficiently high degree ofdifference between two numeric values such that one of skill in the artwould consider the difference between the two values to be ofstatistical significance within the context of the characteristicmeasured by said values. Thus, the difference between two values thatare substantially different from each other is typically greater thanabout 10%, and may be greater than about 20%, preferably greater thanabout 30%, preferably greater than about 40%, preferably greater thanabout 50% as a function of the reference value or comparator value.

Methods, devices, systems, and kits for collecting blood from a digitare disclosed herein. In embodiments, blood may be obtained from a digitby creating a puncture wound or incision through the skin of the digit,effective to allow blood to flow out of the digit for collection. Suchpuncturing or incising of the skin of a digit may be termed a“fingerstick”. Blood obtained by fingerstick from a digit may be termed“fingerstick blood” or a “fingerstick blood sample” or a fingersticksample”. As used herein, a digit may be a finger, or a toe, a heel, anear (e.g., an earlobe), or other body portion.

It will be understood that methods, devices, systems, and kits disclosedherein may be used to obtain fingerstick blood samples from a digit,e.g., from a finger or from a toe of a subject, and in addition may beused to obtain small volume blood samples from, e.g., a heel or othersurface of a subject. In embodiments, such small volume blood samplesobtained from, e.g., a heel or other surface of a subject may beobtained from an infant subject, or a young child, or from an adultsubject suffering from injuries or from a condition which prevents ormakes difficult obtaining a blood sample from a finger or from a toe.

For example, a subject's finger (or toe, or heel, or other portion ofthe subject's body) may be punctured to yield a blood sample. Lancingmay be manually performed, or may be automatically performed. The bloodsample may be collected using a capillary tube, pipette, swab, drop, orany other mechanism known in the art. Blood collection may be manuallyperformed, or may be automatically performed.

A blood sample may be drawn from a subject and provided to a device in avariety of ways, including but not limited to, by fingerstick. Blood maybe liberated from the skin of a subject by lancing with a lancet,needle, or other blade or sharp implement. A sample collector mayinclude a capillary, tube, pipette, syringe, venous draw, or any othercollector. In one embodiment, a lancet punctures the skin and a samplemay be drawn from the wound using, for example, gravity, capillaryaction, aspiration, or vacuum force. A sample collection device willtypically not include a lancet. A sample collection device may bedisposable. In embodiments, a sample collection device may include alancet, which may be disposable. In embodiments, a sample collectiondevice including a lancet may be disposable.

In embodiments, a subject's finger (or other portion of the subject'sbody) may be punctured (i.e., lanced) to yield a blood sample. Puncture(lancing) of a digit may be performed manually. In embodiments, lancingmay be performed automatically. In embodiments, a lancet may beactivated by a variety of mechanical, electrical, electromechanical, orany other known activation mechanism or any combination of such methods.Examples of other portions of the subject's body from which a bloodsample may be collected include, but are not limited to, the subject'shand, wrist, arm, torso, leg, foot, ear, or neck. The blood sample maybe collected using a capillary tube, pipette, or any other mechanismknown in the art. The capillary tube or pipette may be a separatedevice, or may be a part of a device, cartridge, or vessel. Thecollected sample may be placed within a sample analysis device orsystem.

As used herein, a “finger-stick” refers to: i) the act of making a smallpuncture or incision in the skin of a subject, allowing a small amount(e.g., a drop, or one, two, or a few drops) of blood to flow and becomeavailable for collection; ii) the puncture itself; and iii) the bloodcollected thereby. Blood may be liberated in a finger-stick, forexample, by use of a lancet or other sharp implement effective to piercethe skin of a subject. Typically, only a small amount of blood iscollected in this way.

A blood sample obtained from a fingerstick is termed herein a“fingerstick sample”. In embodiments, a fingerstick sample is obtainedfrom a puncture or incision made in a digit, such as a finger, or a toe,of the subject. In embodiments, a fingerstick sample is obtained from apuncture or incision made in any suitable skin surface of a subject,such as, e.g., an ear (e.g., an earlobe), a heel, or other portion of asubject.

In embodiments, a digit may be a finger or toe. In embodiments offingerstick samples obtained from a digit, a puncture, incision, orother wound may be made in a finger tip, or in a tip of a toe, of thesubject. In embodiments, a fingerstick blood sample may be obtained froma heel of a subject, or from an earlobe, or other portion of an ear, orother portion of the body of a subject.

The term “fingerstick blood collection” as used herein refers tocollection of small volume blood samples from a subject, typicallyfollowing use of a lancet to produce a small wound in the skin of asubject. It will be understood that blood may be collected by“fingerstick blood collection” from any portion of a subject's body, andnot only from a finger. For example, in embodiments, blood may becollected from a toe of a subject by “fingerstick blood collection”. Inembodiments, blood may be collected from a heel of a subject by“fingerstick blood collection”. In embodiments, blood may be collectedfrom an ear (e.g., from an earlobe) of a subject by “fingerstick bloodcollection”. In embodiments, blood may be collected from any bodysurface of a subject by “fingerstick blood collection”.

When referring to a volume, e.g., a “finger-stick volume” or “the volumeof a finger-stick”, the term “finger-stick” refers to the volume of afew drops of blood typically obtained from a finger-stick. A single dropof blood may have a volume of about 20-50 μL, e.g., about 40 μL. Thus, afew drops of blood obtained from a finger-stick may provide a volume ofabout 50 μL to about 250 or about 75 μL to about 200 or, in someinstances, between about 100-150 μL. Advantages of obtaining blood froma finger-stick include minimal discomfort to the subject and ease ofaccess, as compared to obtaining blood from a vein or artery. Typically,only a small amount of blood is collected in this way. In embodiments, afingerstick blood sample may be a blood sample having a volume of about300 μL; or about 250 μL; or about 200 μL; or about 175 μL; or about 150μL; or about 125 μL; or about 100 μL; or about 75 μL; or about 50 μL; orabout 45 μL; or about 40 μL; or about 35 μL; or about 30 μL; or about 25μL; or about 20 μL; or about 15 μL; or about 10 μL; or about 5 μL; orother small volume. Blood from a finger-stick may be collected, e.g., byneedle, syringe, capillary tube, sample collection vessel, or by otherimplement or method. Blood from a finger-stick may be collected fortransport to another location; for storage prior to use or analysis; forimmediate use; or for a combination of the same.

As used herein, a “sample” may be a fingerstick blood sample, or may beany small volume blood sample, or may be any blood sample, or a portionof a blood sample. A sample may be of any suitable size or volume, andis preferably of small size or volume. A blood sample may be obtainedfrom a digit (i.e., a finger or a toe); from a heel; from an earlobe; orfrom any other skin surface of a patient. A “fingerstick blood sample”collected from an infant, for example, will typically be collected bylancing a heel of the infant (and such lancing will typically be madewith a shorter lancet, to produce a shallower wound, than would be thecase for an adult subject).

In embodiments of the assays and methods disclosed herein, measurementsmay be made using a small volume blood sample, or no more than a smallvolume portion of a blood sample, where a small volume comprises no morethan about 300 μL; or no more than about 250 μL; or no more than about200 μL; or no more than about 150 μL; or no more than about 100 μL; orno more than about 75 μL; or no more than about 50 μL; or no more thanabout 35 μL; or no more than about 25 μL; or no more than about 20 μL;or no more than about 15 μL; or no more than about 10 μL; or no morethan about 5 μL; or no more than about 3 μL; or no more than about 2 μL;or no more than about 1 μL; or no more than about 0.5 μL.

The term “lancing” as used herein refers to the act of making a smallopening in the skin of a subject; such an opening may be a puncture, oran incision, or other wound which allows blood to flow out of the woundand onto the skin of the subject, providing a sample of blood may bethat may be collected, e.g., for analysis. A wound made by lancing maybe made by a lancet, which may be a needle, a blade, a plurality ofneedles, blades, and combinations thereof. As used herein, a puncture,incision, or other wound is typically a shallow wound, e.g., about 1 or2 millimeters (mm) or less in depth measured form the skin surface (foran adult subject; such a wound for obtaining a blood sample from aninfant may be about 0.5 to about 1 mm in depth, or less).

The term “lancet” as used herein refers to a needle, blade, or othersharp implement used to make a small wound in the skin for obtaining ablood sample, such as a fingerstick blood sample, which is typically asample of capillary blood. A lancet suitable for use on the digit of anadult patient may make a wound of about 1 to 2 millimeters (mm) indepth, and may make a wound of less than about 1 mm in depth for aninfant. The total length of a lancet suitable for making wounds of suchdepths will typically be longer than these depths, e.g., a lancet formaking a wound of about 1 to 2 mm in depth may be about 3 to about 5 mmlong, or longer. The depth of penetration may be limited during lancingby control of the insertion mechanism, by inclusion of a stop or guardon the lancet or on a mechanism holding or otherwise controlling themotion of the lancet, or by other means.

As used herein, a puncture, incision, or other wound is typically ashallow wound, e.g., about 1 or 2 millimeters (mm) or less in depthmeasured from the skin surface.

As used herein, the term “cuff” refers to an inflatable structure havinga partially, or completely, tubular configuration, which may be placedon or around a digit (such as a finger or a toe) with the digit disposedwithin the interior portion of the tubular structure. Where the cuffforms a completely tubular structure, the digit fits within the cuff,with the cuff placed somewhat like a ring around the digit; typically,when in place, a cuff leaves a distal portion of the digit uncoveredeven when inflated. Where the cuff forms a partially tubular structure,the digit fits within the cuff, with the cuff placed around the digitsomewhat like a ring which has a gap; typically, when in place, such acuff also leaves a distal portion of the digit uncovered even wheninflated.

As used herein, the phrases “internal diameter” and “cuff internaldiameter” refer to the distance between one side of the interior wall ofa deflated cuff to the other side of the interior wall of the deflatedcuff. The internal diameter is measured along a diameter (for cuffs ofsubstantially circular cross-section) or along a line that crosses acenter or crosses between centers (for cuffs having substantiallyelliptical or oval cross-sections). An internal diameter may be measuredfor cuffs which are configured to completely encircle a digit (i.e.,cuffs which have cross-sections that form closed loops) and may bemeasured for cuffs which are configured to partially encircle a digit(i.e., cuffs which have cross-sections that do not form closed loops; insuch a case, the internal diameter may be measured from one inner wallto the opposite inner wall across a center, or centers, of a closedcurve which lies substantially along the open cross-sectional curve ofthe cuff interior surface).

Applicant uses the term “pulse” to refer to application of pressure to adigit, constriction of a digit, or compression of a digit. A “pulse” anda “pressure pulse” may be provided by a cuff. Inflation of a cuff,followed by deflation (or decrease in the amount of inflation) providesa pulse. Multiple pulses may be provided during cyclic inflations (wherethe inflations may be separated by periods of deflation); the rate ofproviding such inflations (e.g., once per second, or once per twoseconds, or other rate) is termed the “pulse frequency.” A pulsefrequency may be, for example, at least about 15 cycles per minute, orat least about 20 cycles per minute, or at least about 30 cycles perminute. In embodiments of pulses, the duration of inflation of a cuff issubstantially equal to the duration of deflation of the cuff. Forexample, in embodiments of pulses, the duration of cuff inflation may beabout 1 second, and the duration of cuff deflation may be about 1second. In embodiments of pulses, the duration of cuff inflation may beabout 2 seconds, and the duration of cuff deflation may be about 2seconds. In embodiments of pulses, the duration of inflation of a cuffis different than the duration of deflation of the cuff. For example, inembodiments of pulses, the duration of cuff inflation may be about 2seconds, and the duration of cuff deflation may be about 1 second. Inembodiments of pulses, the duration of cuff inflation may be about 3seconds, and the duration of cuff deflation may be about 1 second.

Devices and systems disclosed herein are configured to, and may be usedto, deliver a “pulse” or a plurality of “pulses” to a digit of asubject. Methods disclosed herein comprise delivery of a “pulse” or of aplurality of “pulses” to a digit of a subject. In embodiments, pulsesmay be delivered to a digit at a particular frequency; in embodiments,pulses may be delivered to a digit at two or more frequencies; inembodiments, pulses may be delivered to a digit at irregular intervals;in embodiments, pulses may be delivered to a digit at random intervals.

As used herein, the term “tourniquet” and the phrase “to tourniquet thepatient's finger” refer to application of pressure (e.g., application ofpressure to a digit) effective to reduce or prevent blood flow out ofthe digit. Constriction of a digit, as may be effected, for example, bymanual squeezing of a digit by two or more fingers of a technician'shand, can reduce or prevent blood flow out of the squeezed digit so thatblood collects in the distal portion of the digit (the portion fartherfrom the palm of the hand or ball of the foot) aiding in collection of ablood sample from that digit after lancing that digit.

An automatic sample analysis device or system may be configured toreceive the sample, whether it be directly from a subject, from a bodilyfluid collector, or from any other mechanism. A sample may be placed ina container for transport to another location; for example, a sample maybe placed in a container for transport to an automatic sample analysisdevice or system at a different location than the sample collectionlocation. A sample in a container may be placed in a cartridge forloading on an automatic sample analysis device or system for processing,for analysis, or both. In embodiments, cartridges containing a sample ina container may also contain reagents for use in analyzing the sample. Asample may be placed within an automatic sample analysis device orsystem. A sample collection unit of the device may be configured toreceive the sample. In some embodiments, a sample may be provideddirectly to an automatic sample analysis device or system, or a vesselor component may be used as a conduit or means for providing a sample toan automatic sample analysis device or system.

Methods, devices and systems for sample analysis may be used to performassays on a sample, or samples, in order to detect, determine, orquantify some characteristic of a sample (such as detecting whether ornot the sample contains a particular analyte, or such as determining theconcentration of a particular analyte present in the sample). In anassay, a sample may be prepared for use, and may be used, in the assayin ways determined by the nature of the target analyte and by the natureand amount of sample available for use in the assay. Steps useful inpreparing a sample for use in an assay may be termed “processing” steps,while steps which make, or are closely linked to making, measurementsregarding the presence, or amount, or concentration of a target analytemay be termed “analyzing” steps.

Thus, sample analysis may include both processing steps and analyzingsteps.

Sample analysis includes processing of a sample, or portion thereof,whether diluted on undiluted. Processing may include, for non-limitingexample, providing, storing, transporting, warming, cooling, freezing,filtering, coagulating, separating, centrifuging, diluting, preserving,and other steps.

Sample analysis also includes analyzing a sample, or portion thereof,whether diluted on undiluted. Analyzing may include, for non-limitingexample, reacting, hybridizing, binding, illuminating, detecting,comparing (e.g., to a standard curve), subtracting (e.g., valuesobtained from a blank), and other steps.

Some steps, such as mixing, sonicating, labeling, incubating, chelating,and other steps, may be considered processing steps, or may beconsidered analyzing steps, or both.

As used herein, a “technician” or a “user” refers to the personoperating the automatic pressure application device or system asdisclosed herein for use on a patient to collect a fingerstick bloodsample.

As used herein, a “patient” or a “subject” is a person from whom theblood sample is being collected and thus on which devices and systemsdisclosed herein is being used. A blood sample may be collected from apatient for any purpose, including, for example, for a routine clinicalcheck-up, for screening purposes, for diagnostic purposes, forconfirmatory purposes, for monitoring purposes, for purposes ofdetermining the effect or metabolism of drugs or other compounds oragents taken by the patient, for purposes of determining the amount ordose of drugs or other compounds or agents to be administered to thepatient, to determine the suitability for drugs or treatmentscontemplated for the patient, and for other reasons.

As used herein, an “adult” refers to an individual whose age is greaterthan 12 years of age. A patient may be an adult patient. A fingersticksample is typically collected from a finger (and typically a fingertip)of an adult patient. In embodiments, a fingerstick sample taken from anadult may be obtained from a toe, or from another portion of the body.

As used herein, a pediatric application or a pediatric use is one forchildren, i.e., individuals of between 2 and 12 years of age. A patientmay be a pediatric patient (i.e., may be between 2 and 12 years of age).In embodiments, a fingerstick sample taken from a pediatric patient maybe obtained from a toe, or from a heel, or from another portion of thebody.

As used herein, an infant is a person of less than 2 years of age. Apatient may be an infant patient. In embodiments, a fingerstick sampletaken from an infant may be obtained from a finger, or from a heel, orfrom a toe, or from another portion of the infant's body.

As used herein, “distal” refers to locations on a digit farther awayfrom the base of the digit, while “proximal” refers to locations on adigit closer to the base of the digit, where the base of a digit is thepalm of the hand for a finger, and is the region near the ball or archof the foot for a toe. For example, the tip of a finger is a distalportion of a finger, and the base of a finger is a proximal portion ofthe finger (e.g., is proximal to the palm of the hand). For example, thetip of a toe is a distal portion of a toe, and the base of a toe is aproximal portion of the toe (e.g., is near to the ball of the foot).Thus, as used herein, a proximal portion of a digit is closer to thepalm of the hand or to the ball of the foot than a distal portion ofthat digit.

As used herein, a “redraw” is a repetition of a sample collectionattempt; such an attempt may be by using a new lancet on a finger, byusing a new needle on a vein, by using a new needle on an artery, or byother means.

As used herein, the term “point of service location” refers to locationswhere a subject may receive a service (e.g. testing, monitoring,treatment, diagnosis, guidance, sample collection, ID verification,medical services, non-medical services, etc.), and may include, withoutlimitation, a subject's home, a subject's business, the location of ahealthcare provider (e.g., doctor), hospitals, emergency rooms,operating rooms, clinics, health care professionals' offices,laboratories, retailers [e.g. pharmacies (e.g., retail pharmacy,clinical pharmacy, hospital pharmacy), drugstores, supermarkets,grocers, etc.], transportation vehicles (e.g. car, boat, truck, bus,airplane, motorcycle, ambulance, mobile unit, fire engine/truck,emergency vehicle, law enforcement vehicle, police car, or other vehicleconfigured to transport a subject from one point to another, etc.),traveling medical care units, mobile units, schools, day-care centers,security screening locations, combat locations, health assisted livingresidences, government offices, office buildings, tents, bodily fluidsample acquisition sites (e.g. blood collection centers), sites at ornear an entrance to a location that a subject may wish to access, siteson or near a device that a subject may wish to access (e.g., thelocation of a computer if the subject wishes to access the computer), alocation where a sample processing device receives a sample, or anyother point of service location described elsewhere herein.

As used herein, a Patient Service Center (PSC) is a retail location atwhich sample collections are or may be performed.

It is to be understood that both the foregoing general description andthe following detailed description are exemplary and explanatory onlyand are not restrictive of the invention, as claimed. It may be notedthat, as used in the specification and the appended claims, the singularforms “a”, “an” and “the” include plural referents unless the contextclearly dictates otherwise. Thus, for example, reference to “a material”may include mixtures of materials, reference to “a compound” may includemultiple compounds, and the like. Also, as used in the descriptionherein and throughout the claims that follow, the meaning of “in”includes “in” and “on” unless the context clearly dictates otherwise.Finally, as used in the description herein and throughout the claimsthat follow, the meaning of “or” includes both the conjunctive anddisjunctive unless the context expressly dictates otherwise. Thus, theterm “or” includes “and/or” unless the context expressly dictatesotherwise.

Fingerstick Blood Collection

Applicant discloses herein methods, devices, systems, and kits forfingerstick blood collection. In embodiments, some or all of such bloodcollection may comprise automated fingerstick blood collection. Thesemethods, devices, systems, and kits are simple and straight-forward touse. These methods, devices, systems, and kits are designed so that noextensive amount of training or experience are required for theirsuccessful use in obtaining fingerstick samples from subjects. Forexample, in embodiments, methods, devices, systems, and kits disclosedherein are designed for use by technicians with little or no priortechnical or medical experience. Thus, the methods, devices, systems,and kits disclosed herein are designed for use by sophisticated and byunsophisticated technicians and phlebotomists, and offer advantagesincluding ease of use and wide applicability.

Typically, fingerstick blood sample collection is performed quickly inorder to obtain the blood sample before partial or complete clotting ofthe lancing site occurs; quick collection (e.g., less than about 100seconds, or less than about 90 seconds, or less than about 80 seconds,or less than about 70 seconds, or less than about 60 seconds) provides afingerstick blood sample of sufficient volume and quality for diagnosticprocessing. In some instances, collecting blood from a fingerstick attimes later than about 80 seconds may lead to collection of blood ofinsufficient quality or integrity for proper blood analysis. Inembodiments, collecting blood from a fingerstick within a time period ofless than about 80 seconds, or less than about 70 seconds, or less thanabout 60 seconds, provides blood of sufficient quality and integrity forproper blood analysis. For example, coagulation of blood increases overtime following wound formation, and so may occur in increasing amountsover time after lancing, reducing (negatively impact) the quality of thesample (due to increasing amounts of coagulation or other sampledegradation), and may reduce (negatively impact) the integrity of theblood sample as coagulation increases and the relative amounts of plasmaor serum in the whole blood alter over time after lancing to obtain thefingerstick blood sample. For further example, excessive leakage ofinterstitial fluid, as may occur in increasing amounts over time afterlancing, may contaminate a blood sample and may reduce (negativelyimpact) the quality of the sample (possibly altering analyteconcentrations, or in other ways reducing the quality of the bloodsample), and may reduce (negatively impact) the integrity of the bloodsample as increasing amounts of contaminating fluid is mixed in with theblood obtained from the fingerstick.

Manual gripping techniques in which pressure is applied cyclically tothe finger during collection following lancing may be used to generateblood drops for collection into a collection tube, or other samplecollection device. Continuous application of pressure to the digit(e.g., constriction of a digit) is believed to improve fingerstick bloodcollection by increasing blood volume in distal portions of a digitafter a sufficient amount of time following application of pressure.Cyclic application of pressure to the digit is believed to improvefingerstick blood collection by increasing blood volume in distalportions of a digit during the time soon after lancing followingcontinuous application of pressure. Such increased blood volume may aidin the collection of sufficient amounts of blood soon after lancing andso avoid or reduce problems which may arise from coagulation, leakage ofinterstitial fluid, or other problems which lead to reduced quality andreduced integrity of fingerstick blood samples. Such cyclic applicationof pressure to the digit during fingerstick blood collection is alsobelieved to reduce discomfort and pain that may otherwise be felt by asubject during or after collection of a fingerstick blood sample.Although effective, manual gripping techniques require training andpractice to execute well.

For example, manual gripping techniques for cyclic application ofpressure to a digit during fingerstick blood sample collection require acertain amount of dexterity and coordination. Training and practice aredesired in order to learn to properly perform such manual grippingtechniques for cyclic application of pressure to a digit duringfingerstick blood sample collection. Improper application of manualgripping techniques for cyclic application of pressure to a digit duringfingerstick blood sample collection may reduce blood flow into the digitand lead to collection of an insufficient volume of blood, or may leadto excessive coagulation of blood during blood collection, or may allowcontamination of the blood sample with excessive amounts of interstitialfluid, or other problems. Such problems may require that a sample bediscarded, and another sample collected; such a “redraw” may beunexpected by the subject, who may find such a “redraw” uncomfortable orundesirable. Discarding a blood sample is wasteful, and obtaining areplacement sample takes further time and expense. In addition, manualapplication of pressure to a digit during fingerstick blood samplecollection may, on occasion, require the technician to use theirnon-dominant hand, and may possibly lead to repetitive motion injurieswith long-term use of such manual grip techniques. Although thecollection time may be an important parameter with regard to samplequality, manual techniques typically provide no feedback to thetechnician regarding how long collection is taking, and may beinconsistent in their application and in their results. Consequently,when pressure is applied to a digit using manual techniques, samplequality issues related to collection speed can be difficult to identifyor trace.

Applicant discloses herein devices and systems for automated applicationof pressure to a digit. Applicant discloses herein devices and systemsfor automated application of pressure to a digit which include automatedcyclic application of pressure to a digit during fingerstick bloodsample collection. The methods, devices, systems, and kits disclosedherein automate the process of cyclic application of pressure to a digitduring fingerstick blood collection. These automated devices and methodsare believed to improve the practice of cyclic application of pressureto a digit as compared to manual methods of cyclic application ofpressure to a digit during fingerstick blood collection. These automateddevices and methods are believed to provide more consistent and morereliable cyclic application of pressure to a digit as compared to manualmethods of cyclic application of pressure to a digit during fingerstickblood collection. These automated devices, systems, kits, and methods ofcyclic application of pressure to a digit during fingerstick bloodcollection are believed to provide better fingerstick blood samples thanare typically obtained using manual methods of cyclic application ofpressure to a digit during fingerstick blood collection. Such betterfingerstick blood samples may be collected sooner (i.e., sufficientvolume of blood may be collected sooner than would typically be the casewith manual methods of cyclic application of pressure to a digit duringfingerstick blood collection). Such better fingerstick blood samples mayhave less coagulation (i.e., as compared to such a fingerstick bloodsample collected using manual methods of cyclic application of pressureto a digit during fingerstick blood collection). Such better fingerstickblood samples may have less contamination by interstitial fluid (i.e.,as compared to such a fingerstick blood sample collected using manualmethods of cyclic application of pressure to a digit during fingerstickblood collection). Such better fingerstick blood samples may be ofhigher quality, or a greater integrity (i.e., as compared to such afingerstick blood sample collected using manual methods of cyclicapplication of pressure to a digit during fingerstick blood collection).The use of automated application of pressure to a digit may furtherallow a technician to focus attention on positioning of a samplecollection device and on collecting a sample without also having tofocus on coordinated application of pressure to the subject. Thus, thepresent automated devices, systems, kits, and methods are believed toprovide advantages over manual methods of cyclic application of pressureto a digit during fingerstick blood collection.

Devices and Systems

Applicant discloses herein devices, systems, methods, and kits usefulfor collecting fingerstick blood samples from a digit (e.g., from afinger or toe). In embodiments, devices for collecting fingerstick bloodsamples provide automated pressure cycling for collection of bloodduring a fixed collection time period. In embodiments, such automatedpressure cycling is provided by an inflatable cuff which fits around adigit, and may be inflated and deflated repeatedly during at least partof the collection time period. In embodiments, devices for collectingfingerstick blood samples provide digit warming as well as automatedpressure cycling for collection of blood during a fixed collection timeperiod. In embodiments, devices for collecting fingerstick blood samplesprovide digit warming and digit lancing as well as automated pressurecycling for collection of blood during a fixed collection time period.

In embodiments, systems for collecting fingerstick blood samples provideautomated pressure cycling for collection of blood during a fixedcollection time period. In embodiments, such automated pressure cyclingis provided by an inflatable cuff which fits around a digit, and may beinflated and deflated repeatedly during the collection time period. Inembodiments, systems for collecting fingerstick blood samples providedigit warming as well as automated pressure cycling for collection ofblood during a fixed collection time period. In embodiments, systems forcollecting fingerstick blood samples provide digit warming and digitlancing as well as automated pressure cycling for collection of bloodduring a fixed collection time period.

In embodiments, a device having features as disclosed herein comprises acuff configured to at least partially encircle a human digit; a pressuresource configured to inflate said cuff effective to apply pressure to adigit disposed at least partially within the cuff; and a timingmechanism configured to provide a signal at the end of a period of time,where said period of time is a desired period of time for collecting afingerstick blood sample from said digit. In embodiments, a timingmechanism of such a device having features as disclosed herein furtherprovides a signal at the beginning of said period of time. Inembodiments, a signal provided by such a timing mechanism may be asignal selected from an audible signal, a visible signal, and a tactilesignal. In embodiments, a timing mechanism signal may be a beep or atone. In embodiments, a timing mechanism signal at the beginning of aperiod of time may be different than the timing mechanism signalprovided at the end of the period of time.

In embodiments, such a period of time is at least about one minute induration. In embodiments, such a period of time is 60 seconds induration. In embodiments, such a timing mechanism is configured to endthe inflation of said cuff at the end of said period of time. Inembodiments, a cuff of a device having features as disclosed herein maybe configured to be inflated to a maximum pressure of about 300 mm ofmercury of pressure. In embodiments, a cuff of a device having featuresas disclosed herein may include a warming mechanism configured to warm adigit disposed within said cuff. In embodiments, a timing mechanism maybe configured to indicate a warming period during which a digit is to bewarmed. In embodiments, a warming period is a period of time of about 45seconds or more. In embodiments, a cuff of a device having features asdisclosed herein may comprises a plurality of lobes, wherein each lobemay be inflated independently of the other lobe or lobes.

In embodiments, a device having features as disclosed herein may includea lancing mechanism. In embodiments, such a lancing mechanism may beconfigured to puncture a digit effective to make a wound or incision insaid digit providing blood for sample collection. In embodiments, such alancing mechanism may be configured to lance a digit disposed withinsaid cuff, without contacting the cuff. In embodiments, such a lancingmechanism may be configured to lance a digit disposed within said cuff,without affecting the cuff, including without puncturing the cuff. Inembodiments, a lancing mechanism includes a needle, a blade, or otherlancing implement configured to produce a puncture or incision in theskin of a subject effective to release capillary blood from theresulting wound. In embodiments, such a wound may be about 1 to 2millimeters (mm) in depth for an adult subject, and may be about 0.5 to1 mm in depth for an infant.

In embodiments, a device having features as disclosed herein may includean automated sample collection device configured to receive a bloodsample obtained from said digit. In embodiments, a device havingfeatures as disclosed herein may include an automated sample analysisdevice configured to dilute a blood sample obtained from said digit. Inembodiments, a device having features as disclosed herein may include anautomated sample analysis device configured to process a blood sampleobtained from said digit. In embodiments, a device having features asdisclosed herein may include an automated sample analysis deviceconfigured to analyze a blood sample obtained from said digit. Inembodiments, such an automated sample analysis device may be configuredto detect, or to measure the concentrations of, a plurality of analytesin said blood sample obtained from said digit. In embodiments, such anautomated sample analysis device is configured to detect, or to measurethe concentrations of, at least two analytes of different analyte typesin said blood sample obtained from said digit, wherein said analytetypes consist of nucleic acid analytes, peptide analytes, small moleculeanalytes, and cellular markers.

In embodiments, a device having features as disclosed herein may includea communication unit effective to transmit data obtained from said bloodsample. In embodiments, such a communication unit may be effective totransmit data obtained from said a blood sample. In embodiments, such acommunication unit is effective to transmit raw data obtained fromprocessing or analysis of the blood sample. In embodiments, such acommunication unit is effective to transmit analysis results obtainedfrom analysis of the blood sample.

In embodiments, a device having features as disclosed herein may includea warming mechanism configured to warm a digit disposed within saidcuff, and a lancing mechanism configured to puncture a digit effectiveto make a wound or incision in said digit providing blood for samplecollection. In embodiments, a device having features as disclosed hereinmay include a pressure-interruption switch. A pressure interruptionswitch is configured to interrupt inflation of a cuff, and may beconfigured to allow deflation of a cuff. In embodiments, a pressureinterruption switch may be operably connected to a source of pressure,or between a source of pressure and an inflatable cuff, effective thatoperation of the pressure interruption switch prevents pressure flow tothe cuff when the switch is activated. In embodiments, a pressureinterruption switch may be operably connected to a pump, effective thatoperation of the pressure interruption switch stops operation of thepump when the switch is activated. In embodiments, a pressureinterruption switch may be operably connected to a conduit connecting asource of pressure to a cuff, effective to block or occlude the conduitto prevent pressure flow to the cuff when the switch is activated. Inembodiments, a pressure interruption switch may be operably connected toa relief valve, effective that operation of the pressure interruptionswitch opens the relief valve and allows deflation of the cuff when theswitch is activated. In embodiments, a pressure-interruption switch is afoot pedal.

In embodiments, a system having features disclosed herein may include adevice having features as disclosed herein, and an automated samplecollection device configured to collect a blood sample from a puncturewound in a digit. In embodiments, a system having features disclosedherein may include a device having features as disclosed herein, and anautomated sample analysis device configured to dilute a blood sample. Inembodiments, a system having features disclosed herein may include adevice having features as disclosed herein, and an automated sampleanalysis device configured to process a blood sample. In embodiments, asystem having features disclosed herein may include a device havingfeatures as disclosed herein, and an automated sample analysis deviceconfigured to analyze a blood sample.

In embodiments, a system having features disclosed herein may include adevice having features as disclosed herein, an automated samplecollection device configured to collect a blood sample from a puncturewound in a digit, and a communication unit effective to transmit dataobtained from said a blood sample. In embodiments, a system havingfeatures disclosed herein may include a device having features asdisclosed herein, an automated sample analysis device configured todilute a blood sample, and a communication unit effective to transmitdata obtained from said a blood sample. In embodiments, a system havingfeatures disclosed herein may include a device having features asdisclosed herein, an automated sample analysis device configured toprocess a blood sample, and a communication unit effective to transmitdata obtained from said a blood sample. In embodiments, a system havingfeatures disclosed herein may include a device having features asdisclosed herein, an automated sample analysis device configured toanalyze a blood sample, and a communication unit effective to transmitdata obtained from said a blood sample.

Applicant discloses herein devices and systems including a cuff and asource of pressure. A cuff is configured to contact and to at leastpartially encircle a digit (or other body part) of a subject. Inembodiments, a cuff may be configured to contact and to at leastpartially encircle a digit (or other body part) while leaving at least aportion of the digit (or other body part) exposed for lancing by alancet, needle, blade, or other lancing device. In embodiments, a sourceof pressure may include a pump, or a reservoir of compressed gas, orother pressure source. A pump may provide air pressure, or liquidpressure, or otherwise provide pressure effective to inflate a cuff. Apump may be or include a rotary pump, a peristaltic pump, a piston, orother source of pressure. A cuff and a source of pressure are operablyconnected, e.g., via conduit, which conduit may regulate the pressureprovided to the cuff by the pressure source (e.g., may prevent, allow,or modulate the application and amount of pressure provided to thecuff). A conduit is typically flexible, and may be hinged, or includejoints or other elements providing mobility and allowing ease ofplacement of a cuff attached to such a conduit. In embodiments, devicesas disclosed herein may include a valve, or a plurality of valves,effective control or modulate the application and amount of pressureprovided to the cuff. In embodiments, devices as disclosed herein mayinclude a pressure regulator effective control or modulate theapplication and amount of pressure provided to the cuff. Application ofpressure to the cuff by the pressure source is effective to inflate thecuff; when a cuff is in place on or around a digit (or other body part),such inflation is effective to compress or constrict at least a portionof the digit or other body part.

For example, a cuff may be placed on a distal portion of a finger (ortoe) of a subject, leaving at least about 5 millimeters (mm) or at leastabout 10 mm of skin exposed on a distal portion of the finger (or toe)and available for lancing. The cuff may be inflated, constricting thefinger (or toe), so as to reduce or prevent blood flow out of a distalportion of the finger (or toe), allowing blood to collect in the distalportion of that finger (or toe). Such collection of blood in the distalportion of that finger (or toe) may be observed by a reddening, ordeepening in color, of that portion of that finger (or toe). Lancing ofthat distal portion of that finger (or toe) provides blood forfingerstick blood sample collection. Warming of the finger (or toe)prior to constriction of the distal portion of that finger (or toe) maybe effective to increase the amount of blood collecting in that distalportion (as compared to the amount collecting in that distal portionwithout prior warming) for fingerstick blood sample collection, mayincrease blood flow out of a wound made by lancing that finger (or toe),and may be effective to reduce the amount of time required to collect adesired amount of blood from that wound following lancing.

In embodiments, such a cuff has a warming element effective to warmfinger in contact with the cuff, or enclosed or encircled by the cuff. Adigit in contact with, or in place within, a cuff may be warmed prior toinflation of the cuff. A digit in contact with, or in place within, acuff may be warmed during inflation of the cuff, and may be warmed whilethe cuff remains inflated, or during cycles of cuff inflation.

In embodiments, lancing of a digit may be performed while the digit isin place within a cuff. Typically, such lancing may occur while the cuffis inflated; in embodiments, such lancing occurs following a period ofcuff inflation. In embodiments, such lancing is performed on a digit inplace within an inflated cuff after the digit has noticeably deepened orreddened in color. In embodiments, such lancing is performed on a digitin place within a cuff at least about 5 seconds following inflation ofthe cuff. In embodiments, such lancing is performed on a digit in placewithin a cuff at least about 10 seconds following inflation of the cuff.In embodiments, such lancing is performed on a digit in place within aninflated cuff following a signal from the device indicating thatsufficient inflation time has passed and lancing may proceed. Inembodiments, such a signal is an audible signal, such as a beep or atone. In embodiments, such lancing is automatically performed on a digitin place within an inflated cuff by an automated lancing mechanism.

In embodiments, collection of a fingerstick blood sample follows lancingof the digit. In embodiments, such collection of a fingerstick bloodsample may be performed manually. In embodiments, such collection of afingerstick blood sample may be performed following a signal from thedevice indicating that blood collection may proceed. In embodiments,such a signal is an audible signal, such as a beep or a tone. Inembodiments, such collection of a fingerstick blood sample may beperformed automatically by an automated sample collection device, or byan automated sample collection system.

Applicant discloses herein devices and systems including a cuff, apressure source, and a timing mechanism, wherein the cuff is configuredto contact and to at least partially encircle a digit of a subject, andto apply pressure to that digit for a period of time. The period of timeduring which a cuff may apply pressure to a digit may be determined bythe timing mechanism, or a timing mechanism may provide a timing signalto aid an operator in identifying a start time for application ofpressure, a duration for application of pressure, a stop time forapplication of pressure, or combinations thereof. Thus, in embodiments,a timing signal may be provided to indicate the beginning of the bloodcollection period; to indicate the end of the blood collection period;and timing signals may be provided indicating the beginning of the bloodcollection period and the end of the blood collection period. Inembodiments, a timing signal may be provided to indicate the beginningof the warming period; to indicate the end of the warming period; andtiming signals may be provided indicating the beginning of the warmingperiod and the end of the warming period. In embodiments, a timingsignal may be provided to indicate the beginning of pressureapplication; to indicate the end of pressure application; and timingsignals may be provided indicating the beginning and end of the timeperiod for pressure application. In embodiments, the time period forpressure application is the time period for continuous pressureapplication; in embodiments, the time period for pressure application isthe time period for cyclic pressure application. In embodiments, atiming signal may be provided to indicate the time of beginning cyclingof pressure application; to indicate the time of ending cycling ofpressure application; and, in embodiments, timing signals may beprovided indicating the beginning and end of the time period for cyclicpressure application. In embodiments, a timing signal may be provided toindicate the proper time to lance a digit and at other times.

Applicant notes that the amount of time taken to collect a fingerstickblood sample may affect the quality of the sample. Collection of bloodfor a fingerstick blood sample is preferably performed soon afterlancing a digit to provide a fingerstick wound from which to collect theblood sample. Blood flowing from a digit from a fingerstick wound iscapillary blood; such blood is suitable for use in a fingerstick bloodsample so long as the blood is not degraded or compromised in quality.Degradation of a fingerstick blood sample occurs, for example, as theblood becomes coagulated; as hemolysis occurs in the blood sample; asinterstitial fluid from tissue around the wound mixes with the bloodsample. Such degradation is non-existent or negligible at short periodsof time following lancing of the digit. However, over a period of time,the blood flowing from the fingerstick wound becomes degraded, andbecomes of lower quality, as indicated above.

A cuff having features as disclosed herein may fit at least partiallyaround a digit, and may completely encircle a digit; in embodiments, thecuff is an inflatable cuff. In embodiments, a cuff may at leastpartially encircle a digit and leave a distal portion of the digituncovered, effective to provide access by a lancet to skin of the digit.In embodiments, a cuff may completely encircle a digit and leave adistal portion of the digit uncovered, effective to provide access by alancet to skin of the digit. In embodiments, a cuff may leave a proximalportion of the digit uncovered. When inflated in place on or around adigit, a cuff is effective to constrict a portion of the digit and tolimit blood flow in the constricted portion. In embodiments, an inflatedcuff, when in place on or around a digit, the cuff is effective to limitblood flow into the constricted portion. In embodiments, an inflatedcuff, when in place on or around a digit, the cuff is effective to limitblood flow out of the constricted portion. Such a cuff may completelyencircle a digit when in place on the digit; or may partially encirclethe digit when in place on the digit. In embodiments, such a cuff may beconfigured to operate with digits ranging in size from about 75 mm toabout 3.5 centimeter (cm) in diameter. In embodiments, such a cuff maybe configured to operate with digits ranging in size from about 1 cm toabout 3 cm in diameter; and may be configured to operate with digitsranging in size from about 1.3 cm to about 2.5 cm diameter.

A cuff configured to operate with digits of a particular size or sizerange is sized to accommodate a digit of that particular size or sizerange: that is, such a cuff (when deflated) has an internal diameterthat is at least that size, or can be stretched to that size, effectiveto allow placement of the cuff around a digit of about that particularsize (when deflated). In embodiments, a cuff has an internal diameter ofbetween about 1 centimeter (cm) and about 3 cm, or has an internaldiameter of between about 1.3 centimeter (cm) and about 2.5 cm (where aninternal diameter is measured across the open area demarked by thecuff). Internal diameter is determined when the cuff is deflated. Wheninflated, the internal diameter of a cuff is smaller than the internaldiameter of the cuff when deflated.

Applicant further discloses herein devices and systems including a cuff,a source of pressure, a means to pulse the application of pressure, anda timing mechanism, wherein the cuff is configured to contact and to atleast partially encircle a digit of a subject, and to apply pressure tothat digit for a period of time. Applicant further discloses hereindevices and systems including a cuff, a source of pressure, a means topulse the application of pressure, and a timing mechanism, wherein thecuff is configured to contact and to at least partially encircle a digitof a subject, and to apply pressure pulses of desired duration, ofdesired frequency, or both, to that digit for a period of time. Inembodiments, such a timing mechanism may be configured to alert a userto the expiration of a period of time. A user may be alerted by anaudible signal, a visible signal, a vibration, or other means andsignals. In embodiments, such an audible signal may be a beep or a tone.In embodiments, such a timing mechanism may be configured to end theapplication of pressure to a digit upon the expiration of a period oftime. In embodiments, such a timing mechanism may be operably connectedwith the pressure source, or with other elements of the devicesdisclosed herein, so as to end the application of pressure pulses to adigit upon the expiration of a period of time. In embodiments, such aperiod of time is an optimal period of time for collecting blood flowingfrom a digit for use in a blood sample. In embodiments, such a period oftime is a period of time during which blood flowing from a digit issuitable for use in a blood sample. In embodiments, such a period oftime is a period of time during which blood flowing from a digit issuitable for use in clinical analysis. In embodiments, such a period oftime is a period of time during which blood flowing from a digit has notsignificantly degraded as compared to a blood sample suitable for use inclinical analysis. In embodiments, such a period of time is a period oftime during which blood flowing from a digit has suitable integrity foruse in a blood sample. In embodiments, such a period of time is a periodof time during which blood flowing from a digit has suitable quality foruse in a blood sample. In embodiments, such a period of time is a periodof time during which blood flowing from a digit is not substantiallycoagulated. In embodiments, such a period of time is a period of timeduring which blood flowing from a digit is not substantially mixed withinterstitial fluid.

In embodiments, such devices and systems may further include apressure-interruption switch, for use by an operator of the devices andsystems, that is configured to pause or stop the application ofpressure. In embodiments, such a pressure-interruption switch may be afoot-pedal switch. In embodiments, such a pressure-interruption switchmay be a hand-operated switch. In embodiments, such apressure-interruption switch may be a voice-activated switch. Inembodiments, such a pressure-interruption switch may be alight-activated switch. In embodiments, such a pressure-interruptionswitch may be operably connected to the pressure source, or to theconduit connecting the pressure source to the cuff, or both, effectiveto stop the pump, or block flow of pressurized gas, or otherwiseinterrupt the provision of pressure to the cuff, temporarily stoppinginflation of the cuff. In embodiments, such a pressure-interruptionswitch may allow deflation of the cuff, by, e.g., opening a relief valvein the cuff, the conduit, or elsewhere, allowing pressure or pressurizedgas to escape, allowing the cuff to deflate, or by other means. Inembodiments, such a pressure-interruption switch may both interrupt theprovision of pressure to the cuff, and allow deflation of the cuff.

In embodiments, such devices and systems may further include a warmingmechanism configured to warm a digit. In embodiments, such a warmingmechanism may be configured to warm at least a portion of a digitwithin, or in contact with, a cuff. In embodiments, such a warmingmechanism may be disposed on or within a cuff. In embodiments, such awarming mechanism, when disposed on or in contact with a digit, maycontact a larger portion of the surface of a digit than does a cuffdisposed on or in contact with that digit. In embodiments, such awarming mechanism may be configured to apply warmth to a digit prior tothe application of pressure to the digit by the cuff. In embodiments,such a warming mechanism may be configured to apply warmth to a digitduring the application of pressure to the digit by the cuff.

In embodiments, such devices and systems may be configured to, and maybe used to, apply pressure to a digit prior to manual lancing of thatdigit. In embodiments, such devices and systems may be configured to,and may be used to, warm a digit and to apply pressure to a digit priorto manual lancing of that digit. In embodiments, such devices andsystems may be configured to, and may be used to, apply pressure to adigit prior to manual collection of a fingerstick blood sample from thatdigit. In embodiments, such devices and systems may be configured to,and may be used to, warm a digit and to apply pressure to a digit priorto collection of a fingerstick blood sample from that digit.

In embodiments, such devices and systems may further include a lancingmechanism configured to puncture a digit effective to make a wound orincision in a digit for providing blood for sample collection. Inembodiments, such a lancing mechanism may be configured to lance aportion of a digit that is not covered by a cuff. In embodiments, such alancing mechanism may be configured to lance a distal portion of adigit. In embodiments, such a lancing mechanism may be configured tolance a digit following application of pressure to the digit by a cuff.In embodiments, such a lancing mechanism may be configured to lance adigit following application of warmth to the digit by a warmingmechanism. In embodiments, such a lancing mechanism may be configured tolance a digit following application of warmth to the digit by a warmingmechanism and following application of pressure to the digit by a cuff.In embodiments, a lancing mechanism includes a needle, a blade, or otherlancing implement configured to produce a puncture or incision in theskin of a subject effective to release capillary blood from theresulting wound. In embodiments, such a wound may be about 1 to 2millimeters (mm) in depth for an adult subject, and may be about 0.5 to1 mm in depth for an infant.

In embodiments, such devices and systems may be configured to, and maybe used to, apply pressure to a digit prior to automatic lancing of thatdigit, and prior to manual collection of a fingerstick blood sample fromthat digit. In embodiments, such devices and systems may be configuredto, and may be used to, warm a digit and to apply pressure to a digitprior to automatic lancing of that digit, and prior to collection of afingerstick blood sample from that digit.

In embodiments, such devices and systems may further include a bloodsample collection mechanism configured to collect blood flowing from apuncture or incision in a digit. In embodiments, such a blood samplecollection mechanism may be configured to collect blood flowing from apuncture or incision in a digit following application of pressure to thedigit by a cuff. In embodiments, such a blood sample collectionmechanism may be configured to collect blood flowing from a puncture orincision in a digit following application of warmth to the digit by awarming mechanism. In embodiments, such a blood sample collectionmechanism may be configured to collect blood flowing from a puncture orincision in a digit following application of warmth to the digit by awarming mechanism and following application of pressure to the digit bya cuff. In embodiments, lancing of a digit may be performed manually, ormay be performed by a device, including by a device having features asdisclosed herein.

In embodiments, such devices and systems may further include anautomated sample analysis device or an automated sample analysis system.Such an automated sample analysis device or automated sample analysissystem is configured to receive a blood sample, and to perform at leastone blood analysis test on the sample. In embodiments, such automatedsample analysis devices or automated sample analysis systems maydirectly receive blood from a digit following application of pressure bya cuff and following lancing of the digit contacted by, or encircled by,a cuff of a device or system as disclosed herein. In embodiments, suchautomated sample analysis devices or automated sample analysis systemsmay receive blood collected from a digit following application ofpressure by a cuff and following lancing of the digit contacted by, orencircled by, a cuff of a device or system as disclosed herein, wheresuch blood is transferred from a device or system comprising a cuff. Inembodiments, such a transfer of blood is effected within a singlehousing which includes a cuff, a pressure source, and a timer as well asan automated sample analysis device or automated sample analysis system.In embodiments, such a transfer of blood is effected between a device orsystem which includes a cuff, a pressure source, and a timer asdisclosed herein, and an automated sample analysis device or automatedsample analysis system, where the device or system which includes acuff, a pressure source, and a timer is separate from the automatedsample analysis device or automated sample analysis system. Inembodiments, such devices and systems may include a transport mechanismor transport system effective to transport a blood sample from a bloodcollection mechanism to an automated sample analysis device or anautomated sample analysis system.

In embodiments, a device or system as disclosed herein, which comprisesan automated sample analysis device or an automated sample analysissystem in addition to a cuff and a pressure source, may also include oneor more of a pressure-interruption switch, a timing mechanism, a warmingmechanism, a lancing mechanism, a blood collection mechanism, and othermechanisms.

In embodiments, a device or system as disclosed herein, which comprisesan automated sample analysis device or an automated sample analysissystem in addition to a cuff, a pressure source, and a timer, may alsoinclude one or more of a pressure-interruption switch, a warmingmechanism, a lancing mechanism, a blood collection mechanism, and othermechanisms.

In embodiments, a device or system as disclosed herein comprising a cuffand a pressure source, may also include one or more of apressure-interruption switch, a timing mechanism, a warming mechanism, alancing mechanism, a blood collection mechanism, and other mechanisms,and may in addition include a communication unit effective to transmitdata regarding a blood sample. In embodiments, a device or system asdisclosed herein which comprises an automated sample analysis device oran automated sample analysis system in addition to comprising a cuff anda pressure source, may also include one or more of apressure-interruption switch, a timing mechanism, a warming mechanism, alancing mechanism, a blood collection mechanism, and other mechanisms.

In embodiments, a device or system as disclosed herein comprising acuff, a pressure source, and a timer, may also include one or more of apressure-interruption switch, a warming mechanism, a lancing mechanism,a blood collection mechanism, and other mechanisms, and may in additioninclude a communication unit effective to transmit data regarding ablood sample. In embodiments, a device or system as disclosed hereinwhich comprises an automated sample analysis device or an automatedsample analysis system in addition to comprising a cuff, a pressuresource, and a timer, may also include one or more of apressure-interruption switch, a warming mechanism, a lancing mechanism,a blood collection mechanism, and other mechanisms.

The devices and systems disclosed herein may include elements configuredto contact a digit and to compress or apply pressure to at least aportion of that digit. In embodiments, devices and systems disclosedherein may include elements configured to encircle a digit and tocompress or apply pressure to at least a portion of that digit. Inembodiments, devices and systems disclosed herein may include elementsconfigured to contact, or to encircle, or both, a digit and to compressor apply pressure to at least a portion of that digit for a period oftime. In embodiments, devices and systems disclosed herein may includeelements configured to contact, or to encircle, or both, a digit and tocompress or apply pressure to at least a portion of that digit for aplurality of periods of time, wherein said plurality of periods of timemay be separated by a time period during which compression or pressureis not applied to the digit. In embodiments, devices and systemsdisclosed herein may include elements configured to contact, or toencircle, or both, a digit and to repeatedly compress or apply pressureto at least a portion of that digit at a defined frequency ofapplication of compression or pressure; in embodiments, periods of timeduring which compression or pressure is applied may be separated by timeperiods during which compression or pressure is not applied to thedigit. In some embodiments, the frequency of application of pressure orcompression to a digit may be unvarying; and, in other embodiments, thefrequency of application of pressure or compression to a digit may vary.In some embodiments, the duration of time periods during whichcompression or pressure is not applied to the digit may be unvarying;and, in other embodiments, the duration of time periods during whichcompression or pressure is not applied to the digit may vary.

In embodiments, the devices and systems disclosed herein provideautomation of the finger pressurizing process during fingerstick bloodcollection in order to eliminate the dependency on, and the variabilitydue to, differences between the grip techniques used by differenttechnicians, and due to differences in application of a grip techniqueby an individual technician as applied to different subjects. Themethods, devices, systems and kits disclosed herein are designed tominimize the amount of technician training that may be required toreproducibly extract blood from the finger of a subject duringfingerstick blood collection, to control the total time allowed forfingerstick blood collection, and in other ways improve standardizationand consistency of the collection process.

Embodiments of the automated fingerstick blood collection methods,devices, systems, and kits disclosed herein include devices, and the useof devices, which provide automated pressure application to a digit(e.g., a finger), with automatic cycling of such pressure between a lowpressure (which may include no added pressure, or may include a smallamount of pressure application) and a high pressure (which may include apressure sufficient to completely occlude, and may include a pressurethat does not completely occlude, blood flow out of the extremity.

Embodiments of the automated fingerstick blood collection methods,devices, systems, and kits disclosed herein include devices, and the useof devices, which provide 1) automatic application of heat to a digit(e.g., a finger), and 2) automated pressure application to a digit(e.g., a finger), with automatic cycling of such pressure between a lowpressure (which may include no added pressure, or may include a smallamount of pressure application) and a high pressure (which may include apressure sufficient to completely occlude, and may include a pressurethat does not completely occlude, blood flow out of the extremity.

Embodiments of the automated fingerstick blood collection methods,devices, systems, and kits disclosed herein include devices, and the useof devices, which provide 1) automatic application of heat to a digit(e.g., a finger), 2) automatic lancing of the extremity, and 3)automated pressure application to a digit (e.g., a finger), withautomatic cycling of such pressure between a low pressure (which mayinclude no added pressure, or may include a small amount of pressureapplication) and a high pressure (which may include a pressuresufficient to completely occlude, and may include a pressure that doesnot completely occlude, blood flow out of the extremity.

Devices, Systems, and Kits

FIG. 1 shows a perspective view of an exemplary device 10 havingfeatures as disclosed herein, including a pressure cuff 40 attached to aconduit 38 and thereby to a control unit 12 having a housing 22, thecontrol unit including a pump effective to apply pressure to the cuffunder the control of the control unit, and a power cable 34 forconnecting a power supply within the housing 22 to a power source (e.g.,an electrical cable 34 with plug 35 for connecting to an electricalpower outlet).

FIG. 2A is a schematic diagram showing elements of an exemplary device10 as disclosed herein, including a housing 22 with an ON/OFF switch 24and containing a pressure source 26, a timer 28, a signal source 30, apower supply 32 connected to a power cable 34, and a link to aninterrupt switch 36. A conduit 38 connects cuff 40 to the pressuresource 26. In embodiments, pressure source 26 may be controlled by, oris under the control of, timer 28. In embodiments, application ofpressure to a cuff 40 by pressure source 26 may be interrupted by aninterrupt switch 36. An interrupt switch 36 may be configured to beoperated with minimal interference with collection of a fingerstickblood sample; for example an interrupt switch 36 may be a foot pedal,which a technician may operate at the same time that technician iscollecting blood from a subject without requiring the use of a hand tointerrupt pressure application. An interrupt switch 36 configured tointerrupt pressure application is optional; some embodiments of thedevices disclosed herein may lack an interrupt switch 36.

In operation, pressing the ON/OFF switch 24 may begin timing of a timer28 and may turn on, or begin, a protocol leading to the turning on of, apressure source 26 effective to inflate cuff 40. In use, a digit of asubject will be placed within a cuff 40, and inflation of the cuff 40will constrict the digit placed therein. A signal may be generated upon,or soon after, pressing the ON/OFF switch 24. In embodiments, pressuremay be applied to a cuff 40 for a continuous period of time duringoperation. In embodiments, pressure applied to a cuff 40 may cyclebetween inflated and deflated conditions. In embodiments, pressureapplied to a cuff 40 may cycle between inflated and deflated conditionsat a set frequency; or at a variable frequency; or for variable amountsof time. In embodiments, pressure applied to a cuff 40 may be heldconstant for a period of time, and may subsequently cycle betweeninflated and deflated conditions for a period of time. In embodiments,pressure applied to a cuff 40 may cycle between inflated and deflatedconditions for a period of time, and may subsequently be held constantfor a period of time.

FIG. 2B is a schematic diagram showing elements of an exemplary device10 as disclosed herein, including a housing 22 with an ON/OFF switch 24and containing a pressure source 26 connected via a conduit 38 to a cuff40 configured to constrict a digit, the cuff including a warming element42, a timer 28, a signal source 30, a power supply 32 connected to apower cable 34, and an (optional) link to a foot pedal (interruptswitch) 36. A conduit 38 connects cuff 40 to the pressure source 26.

FIG. 2C is a schematic diagram showing elements of an exemplary device10 as disclosed herein, including a housing 22 with an ON/OFF switch 24and containing a pressure source 26 connected via a conduit 38 to a cuff40 configured to constrict a digit, the device including a lancingdevice 44, a timer 28, a signal source 30, a power supply 32 connectedto a power cable 34, and an (optional) link to a foot pedal (interruptswitch) 36. In embodiments, the cuff 40 may include a warming element(not shown in the figure). A conduit 38 connects cuff 40 to the pressuresource 26.

FIG. 2D is a schematic diagram showing elements of an exemplary device10 as disclosed herein, including a housing 22 with an ON/OFF switch 24and containing a pressure source 26 connected via a conduit 38 to a cuff40 configured to constrict a digit, a timer 28, a signal source 30, apower supply 32 connected to a power cable 34, a communication element46, and an (optional) link to a foot pedal (interrupt switch) 36. Inembodiments, the cuff 40 may include a warming element (not shown in thefigure). A conduit 38 connects cuff 40 to the pressure source 26.

FIG. 2E is a schematic diagram showing elements of an exemplary device10 as disclosed herein, including a housing 22 with an ON/OFF switch 24and containing a pressure source 26 connected to a cuff 40 configured toconstrict a digit by a conduit 38, a timer 28, a signal source 30, alancing device 44, a sample collection element 48, a power supply 32connected to a power cable 34, and an (optional) link to a foot pedal(interrupt switch) 36. In embodiments, the cuff 40 may include a warmingelement (not shown in the figure). A conduit 38 connects cuff 40 to thepressure source 26.

Embodiments of devices as disclosed herein may include an ON/OFF switch(e.g., an ON/OFF switch 24 as shown in the figures). In embodiments,separate switches may individually perform ON and OFF functionsindependently of each other. In embodiments, further switches may beincluded in devices as disclosed herein.

A cuff (e.g., a cuff 40 as shown in the figures) is configured to beplaced on or around a digit (e.g., a finger or toe) of a subjecteffective to compress a portion of the digit to constrict blood flow,effectively limiting blood flow out of the portion of the digit that isdistal to the cuff. (As used herein, “distal” refers to locations on adigit farther away from the base of the digit, while “proximal” refersto locations on a digit closer to the base of the digit, where the baseof a digit is the palm of the hand for a finger, and is the region nearthe ball or arch of the foot for a toe.) In embodiments, a cuff (when inplace) may completely encircle a digit. When properly placed for use asdisclosed herein, a cuff leaves at least a distal portion of a digituncovered and exposed so as to provide a skin surface suitable forlancing in order to provide a fingerstick blood sample. In embodiments,about 5-10 mm of skin surface of a digit may be left exposed to providea skin surface suitable for lancing. In embodiments, about 5 mm of skinsurface of a digit may be left exposed to provide a skin surfacesuitable for lancing. In embodiments, more than about 10 mm of skinsurface of a digit may be left exposed to provide a skin surfacesuitable for lancing.

A cuff (e.g., a cuff 40 as shown in the figures) is configured toinflate effective to constrict a digit, such as a finger, on or aroundwhich the cuff is disposed. A pressure source may be any suitablepressure source. Pressure for inflating the cuff may be air (or othergas) pressure, or may be fluid pressure (e.g., water, oil, or otherfluid), or other pressure. Pressure for inflating the cuff is suppliedby a pressure source (e.g., a pressure source 26 as shown in thefigures). Any suitable pressure source may be used to provide pressurefor inflating a cuff. A pressure source may be an electric pump, such asa rotary pump, or may be a peristaltic pump, or may include a piston, ormay include other means or elements for producing pressure. A pressuresource may include a combination or variety of pumps and pumpmechanisms. In embodiments, a pressure source may be or may include acontainer holding compressed gas (e.g., a tank of compressed gas, suchas compressed nitrogen, carbon dioxide, or other gas). A pressure sourcemay be operably connected to the cuff by, e.g., a conduit (e.g., aconduit 38 as shown in the figures). A conduit may be a flexibleconduit. A conduit may be made with any material, or combination ofmaterials, which is capable of enclosing gas or fluid withoutsignificant loss of pressure, effective to allow a pressure source topressurize a cuff and to inflate the cuff.

In embodiments, a cuff (e.g., a cuff 40 as illustrated in the figures)may include a warming element (e.g., a warming element 42 as illustratedin the figures), or may have a warming element (e.g., a warming element42 as illustrated in the figures) attached. A warming element may be anysuitable warming element. For example, a warming element may be, or mayinclude, a heating coil (e.g., an electric heating coil). Inembodiments, a heating coil may be embedded in a cuff, or may be placedaround an exterior portion of a cuff, or may be placed on an interiorportion of a cuff, or may be attached to an interior portion of a cuff,or to an exterior portion of a cuff, or to a distal portion or end of acuff, or to a proximal portion or end of a cuff. A warming mechanism maybe configured to warm a digit to about 2° C. above normal skintemperature, or to about 3° C. above normal skin temperature, or toabout 4° C. above normal skin temperature, or to about 5° C. abovenormal skin temperature, or to about 7° C. above normal skintemperature, or to about 9° C. above normal skin temperature, or toabout 10° C. above normal skin temperature, or to about 12° C. abovenormal skin temperature, or higher. A warming mechanism may becontrolled, effective that a user of the device may adjust the amount ofwarming provided by the warming mechanism. For example a warmingmechanism may be adjustable so that a user of the device may adjust thetemperature to which the skin of the digit is to be warmed. Inembodiments, the warming mechanism is operably connected to the timingmechanism, effective that warming may be provided for a set period oftime; in embodiments, such a set period of time may be controlled by atimer.

In embodiments, other warming elements may be used with, or in place of,a heating coil. For example, a warming element may be, or may include, achemical heating element (e.g., a chemical compound or material whichprovides heat, such as, for example, a super-saturated solution ofsodium acetate). In embodiments, a warming element may be, or mayinclude, a tube or conduit for carrying heated oil or other heatedliquid to the cuff. Such warming elements may be embedded in a cuff, ormay be placed around an exterior portion of a cuff, or may be placed onan interior portion of a cuff, or may be attached to an interior, or anexterior, or a distal, or a proximal portion of a cuff.

In embodiments, a timer (e.g., a timer 28 as illustrated in the figures)may include any suitable timing element or timing circuit effective todetermine a period of time, or to measure a period of time, or todetermine or measure a duration, or to provide a frequency (e.g., toprovide a sequence of signals or waveforms at a desired frequency). Atimer may be any suitable timer or timing element.

In embodiments, a signal source (e.g., a signal source 30 as illustratedin the figures) may be any suitable signal source or signaling element,and may produce any suitable signal. In embodiments, a signal source mayprovide an audible signal. In embodiments, a signal may be, or mayinclude, an audible signal, where an audible signal is a signal that maybe heard by a person with normal hearing. In embodiments, an audiblesignal may be a beep, or a click, or a chirp, or a tone, or acombination of tones, or a siren, or other sound. In embodiments, asignal source may provide a visible signal. In embodiments, a signal maybe, or may include, a visible signal, where a visible signal is a signalthat may be seen by a person with normal vision. In embodiments, avisible signal may be a light signal of any color, and may be a briefflash of light, or may be a flashing light (e.g., alternatingillumination and extinction (or diminution) of a light signal), or maybe a sustained light signal. In embodiments, a signal may be, or mayinclude, a tactile signal, where a tactile signal is a signal that maybe felt by a person with normal touch or somatosensory sensitivity. Inembodiments, a tactile signal may be a contact signal (in which, e.g., asignal element normally not in contact with a technician is moved intoplace effective to contact the technician, or a signal element normallyin contact with a technician is moved across or in relation to thetechnician so as to be felt by the technician); may be a pressure signal(in which, e.g., the contact pressure of a signal element normally incontact with a technician is altered by an increase in pressure or adecrease in pressure); or may be a vibration signal, in which avibration produced by the signal source may be felt by the technician.

In embodiments, a power supply (e.g., a power supply 32 as illustratedin the figures) may be any suitable power supply, and may produce anysuitable type and amount of power for use by the device. In embodiments,a power supply may be, e.g., an electric power supply. In embodiments, apower supply may be, e.g., an alternating current electric power supply,suitable for use with standard wall sockets. In embodiments, a powersupply may be, or may include, e.g., a direct current electric powersupply, suitable for use with standard batteries, or rechargeablebatteries, or other electrical power source that does not requirecontinuous connection to a wall socket during use.

In embodiments, an interrupt switch may be any interrupt switcheffective to provide an interrupt command effective to temporarily pauseapplication of pressure to the cuff, or effective to temporarily releasepressure in the cuff. For example, an interrupt switch may be a footpedal which, when stepped on, provides an electrical signal effective tointerrupt application of pressure to the cuff.

In embodiments, a lancing device (e.g., a lancing device 44 asillustrated in the figures) may be any suitable lancing device orlancing element effective to lance a digit to provide a fingerstickwound for collection of a fingerstick blood sample. A lancing device mayinclude a blade (e.g., a lancet) or a needle, or other sharp surface orsharp element configured to provide a small wound in the skin of asubject for releasing drops of blood.

A sample collection device or element (e.g., a sample collection element48 as illustrated in the figures) may be any device or elementconfigured to collect small amounts of blood. In embodiments, a samplecollection device or element is configured to collect a fingerstickblood sample. In embodiments, a sample collection device may beautomatic sample collection device. An automatic sample collectiondevice may be any suitable automatic device which may collect afingerstick sample from a subject. In embodiments, a sample collectiondevice may be configured to work in conjunction with a lancing device asdisclosed herein.

In embodiments, a communication link or communication element (e.g., acommunication link 46 as illustrated in the figures) may be any suitablecommunication link or communication element. In embodiments, acommunication link may be effective to communicate device statusinformation from a device as disclosed herein to an external device, orto a laboratory, or to a network. In embodiments, a communication linkmay be effective to communicate device performance information from adevice as disclosed herein to an external device, or to a laboratory, orto a network. In embodiments, a communication link may be effective tocommunicate device error or failure information from a device asdisclosed herein to an external device, or to a laboratory, or to anetwork. In embodiments, a communication link may be effective tocommunicate data, such as raw data, from a device as disclosed herein toan external device, or to a laboratory, or to a network. In embodiments,a communication link may be effective to communicate raw data from adevice as disclosed herein to a laboratory for performing sampleanalysis. In embodiments, a communication link may be effective tocommunicate data, such as image data, from a device as disclosed hereinto an external device, or to a laboratory, or to a network. Inembodiments, a communication link may be effective to communicate imagedata, from a device as disclosed herein to a laboratory for performingsample analysis. In embodiments, a communication link may be effectiveto communicate data, such as data from analysis of a sample, from adevice as disclosed herein to an external device, or to a laboratory, orto a network. In embodiments, a communication link may be effective tocommunicate data from analysis of a sample from a device as disclosedherein to a laboratory for performing sample analysis.

FIG. 3A is a schematic diagram showing elements of an exemplary system100 including a device 10 as shown in FIGS. 1 and 2B-2E, the device 10including a housing 22 with an ON/OFF switch 24 and containing apressure source 26 connected via a conduit 38 to a cuff 40 configured toconstrict a digit, a timer 28, a signal source 30, a sample collectionelement 48, a power supply 32 connected to a power cable 32, and an(optional) link to a foot pedal (interrupt switch) 36. In embodiments,the cuff 40 may include a warming element (not shown in the figure). Inaddition to the device 10 within and associated with the housing 22, thesystem 100 includes an automatic sample analysis device 50. A conduit 38connects cuff 40 to the pressure source 26.

FIG. 3B is a schematic diagram showing elements of an exemplary system100 including a device 10 as disclosed herein, the device 10 including ahousing 22 with an ON/OFF switch 24 and containing a pressure source 26connected via a conduit 38 to a cuff 40 configured to constrict a digit,a timer 28, a signal source 30, a lancing device 44, a sample collectionelement 48, a power supply 32 connected to a power cable 34, and an(optional) link to a foot pedal (interrupt switch) 36. In embodiments,the cuff 40 may include a warming element (not shown in the figure). Inaddition to the device 10 within and associated with the housing, thesystem 100 includes an automatic sample analysis device 50. A conduit 38connects cuff 40 to the pressure source 26.

An automatic sample analysis device 50 may be any suitable automaticsample analysis device which may be used to analyze, or to aid in theanalysis of, a fingerstick sample collected from a subject. An automaticsample analysis device 50 may be configured to detect the presence of ananalyte in a blood sample. An automatic sample analysis device 50 may beconfigured to measure the amount of an analyte in a blood sample. Anautomatic sample analysis device 50 may be configured to measure aproperty of a blood sample. In embodiments, a property of a blood samplemay be, for example, the pH of a blood sample, the coagulation time of ablood sample, the hematocrit of a blood sample, the amount or percentageof blood oxygenation of a blood sample, and other properties. Exemplaryautomatic sample analysis devices are described, for example, in U.S.Pat. No. 8,380,541; U.S. Pat. No. 8,840,838; U.S. Pat. No. 8,435,738;U.S. Pat. No. 8,475,739; and U.S. patent application Ser. No. 14/183,503filed Feb. 18, 2014, the entire contents of which patents and patentapplications are hereby incorporated by reference in their entireties.

Methods

In embodiments, a method for collecting blood from a digit comprises atleast partially encircling a human digit with a cuff of a device asdisclosed herein; inflating said cuff effective to apply pressure tosaid digit; lancing said digit effective to puncture the skin of thedigit and to allow blood to flow out of the digit; and collecting of atleast a portion of said blood flowing out of the digit. In embodimentsof methods for collecting blood from a digit as disclosed herein,inflation of the cuff is inflation to a maximum pressure of about 300 mmof mercury of pressure. In embodiments, a method for collecting bloodfrom a digit, collecting of at least a portion of said blood flowing outof the digit comprises beginning collection of at least a portion ofsaid blood flowing out of the digit; and ending collection of bloodflowing out of said digit pursuant to a signal from said device. Inembodiments, a method for collecting blood from a digit as disclosedherein comprises use of a device as disclosed herein, wherein the devicecomprises a timing mechanism configured to determine a period of time,and wherein said period of time is a desired period of time forcollecting a fingerstick blood sample from said digit. In embodiments, amethod for collecting blood from a digit as disclosed herein furthercomprise providing a signal at the end of such a period of time. Inembodiments, such a period of time is at least about one minute induration. In embodiments, such a period of time is 60 seconds induration. In embodiments, a method for collecting blood from a digit asdisclosed herein further comprise providing a signal at the beginning ofsaid period of time. In embodiments, a method for collecting blood froma digit as disclosed herein further comprise ending inflation of saidcuff at the end of said period of time. In embodiments of methods forcollecting blood from a digit as disclosed herein, the signal comprisesa signal selected from an audible signal, a visual signal, and a tactilesignal. In embodiments of methods for collecting blood from a digit asdisclosed herein, the signal comprises an electronic, hydraulic, ormechanical signal effective to end the collection of blood flowing outof said digit. In embodiments of methods for collecting blood from adigit as disclosed herein, the signal comprises an electronic,hydraulic, or mechanical signal operably connected to a samplecollection mechanism effective to end the collection of blood flowingout of said digit. In embodiments, a device as disclosed hereincomprises a sample collection mechanism that comprises, or is operablyconnected to, an electronic, hydraulic, or mechanical mechanism orelement that is configured to provide a signal to end the collection ofblood flowing out of a digit, or is configured to directly end thecollection of blood flowing out of a digit. In embodiments, a system asdisclosed herein comprises a device comprising a cuff as disclosedherein, the system further comprising a sample collection device thatcomprises, or is operably connected to, an electronic, hydraulic, ormechanical mechanism or element that is configured to provide a signalto end the collection of blood flowing out of a digit, or is configuredto directly end the collection of blood flowing out of a digit.

In embodiments of methods for collecting blood from a digit as disclosedherein, the methods further comprise warming the digit. In embodimentsof methods for collecting blood from a digit as disclosed herein, thecuff comprises a warming mechanism configured to warm a digit disposedwithin said cuff, and said warming is effected at least in part by saidwarming.

In embodiments of methods for collecting blood from a digit as disclosedherein, the device comprises a lancing mechanism configured to puncturea digit effective to make a wound or incision suitable for providingblood for sample collection, said cuff at least partially encircling ahuman digit, the method comprising lancing said digit with said lancingmechanism. In embodiments, such lancing is performed without contactingthe cuff. In embodiments, such lancing is performed without puncturingthe cuff. In embodiments, such lancing is automatically performed by adevice. In embodiments, such lancing is automatically performed by adevice, where that device is an automatic sample collection device. Inembodiments, such lancing is automatically performed by a device, wherethat device is an automated sample collection device connected with, orpart of, an automated sample analysis device.

In embodiments of methods for collecting blood from a digit as disclosedherein, the device comprises an automated sample collection device, andsaid method comprises automatically collecting the blood sample. Inembodiments of methods for collecting blood from a digit as disclosedherein, the device comprises an automated sample collection device, andsaid method comprises diluting the blood sample. In embodiments ofmethods for collecting blood from a digit as disclosed herein, thedevice comprises an automated sample collection device, and said methodcomprises processing the blood sample. In embodiments of methods forcollecting blood from a digit as disclosed herein, the device comprisesan automated sample collection device, and said method comprisesanalyzing said blood sample.

In embodiments, the methods disclosed herein utilize a device havingfeatures as disclosed herein, the methods comprising use of a firstdevice, wherein the first device comprises a communication uniteffective to transmit data regarding a blood sample, and the methodcomprises transmitting data regarding said blood sample to a seconddevice. In embodiments, such data is raw data obtained from the bloodsample. In embodiments, such data is raw data obtained from processingof the blood sample. In embodiments, such data is raw data obtained fromprocessing the blood sample in an automated sample analysis device. Inembodiments, such data is analysis data obtained from the blood sample.In embodiments, such data is analysis data obtained from analyzing theblood sample. In embodiments, such data is analysis data obtained fromanalyzing the blood sample in an automated sample analysis device.

The methods disclosed herein include methods in which a digit of asubject is contacted, or is encircled, or both, by a cuff of a device orsystem disclosed herein. In embodiments of the methods disclosed herein,a digit of a subject is contacted, or is encircled, or both, by a cuffof a device or system disclosed herein and pressure is applied to atleast a portion of that digit, or at least a portion of the digit iscompressed, by the cuff as disclosed herein. In embodiments of themethods disclosed herein, a digit of a subject is lanced (punctured orotherwise wounded, effective to provide a passage for the flow of thatsubject's blood out of that digit); that digit is contacted, or isencircled, or both, by a cuff of a device or system disclosed herein;and pressure is applied to at least a portion of that digit, or at leasta portion of the digit is compressed, by the element of a device orsystem disclosed herein, while blood flows from the lanced digit of thesubject.

In embodiments of the methods disclosed herein, a digit of a subject ispunctured, incised, or otherwise wounded, effective to provide a passagefor the flow of that subject's blood out of that digit; a pulse ofpressure is applied to that digit, by a cuff of a device or systemdisclosed herein effective that pressure or compression is applied to atleast a portion of that digit, by the cuff, effective to allowcollection of blood in the digit from which a fingerstick sample ofblood is collected. In embodiments, the pulse of pressure is a constantpulse of pressure, and may be maintained during all or during part ofthe period of blood collection.

In embodiments of the methods disclosed herein, a digit of a subject ispunctured, incised, or otherwise wounded, effective to provide a passagefor the flow of that subject's blood out of that digit; that digit iscontacted, or is encircled, or both, by a cuff of a device or systemdisclosed herein; and pressure is applied to at least a portion of thatdigit, or at least a portion of the digit is compressed, for a pluralityof periods of time, wherein said plurality of periods of time may beseparated by a time period during which compression or pressure is notapplied to the digit, by the element of a device or system disclosedherein, while blood flows from the digit of the subject. In embodimentsof the methods disclosed herein, a digit of a subject is punctured orotherwise wounded, effective to provide a passage for the flow of thatsubject's blood out of that digit; that digit is contacted, or isencircled, or both, by an element of a device or system disclosedherein; and pressure is applied to at least a portion of that digit, orat least a portion of the digit is compressed, for a plurality ofperiods of time, wherein said plurality of periods of time may beseparated by a time period during which compression or pressure is notapplied to the digit, by the element of a device or system disclosedherein, effective to express blood from the digit of the subject. Thus,in embodiments, the pulse of pressure is cycled, so that pulses ofpressure to the digit are applied, and pressure is released, in a cyclicmanner; such pulse cycling may be maintained during all or during partof the period of blood collection. In embodiments, such pulse cyclingmay be regular in its application (i.e., each period of cuff inflationis of substantially the same duration as the other periods of cuffinflation, and each period of cuff deflation is of substantially thesame duration as the other periods of cuff deflation). In embodiments,such pulse cycling may be irregular in its application (i.e., a periodof cuff inflation may be of different duration than other periods ofcuff inflation, and a period of cuff deflation may be of differentduration than other periods of cuff deflation).

In embodiments of the methods disclosed herein, a digit of a subject ispunctured or otherwise wounded, effective to provide a passage for theflow of that subject's blood out of that digit, and pressure may berepeatedly applied to at least a portion of that digit at a definedfrequency of application of compression or pressure; in embodiments,periods of time during which compression or pressure is applied may beseparated by time periods during which compression or pressure is notapplied to the digit. In some embodiments, the frequency of applicationof pressure or compression to a digit may be unvarying; and, in otherembodiments, the frequency of application of pressure or compression toa digit may vary. In some embodiments, the duration of time periodsduring which compression or pressure is not applied to the digit may beunvarying; and, in other embodiments, the duration of time periodsduring which compression or pressure is not applied to the digit mayvary. In such embodiments, the repeated contact with the digit, orrepeated application of pressure to the digit, may be performed whileblood flows from the digit of the subject. In such embodiments, therepeated contact with, or repeated application of pressure to, the digitmay be effective to increase the amount of blood collected from thedigit of the subject, or to decrease the amount of time required tocollect a desired amount of blood, as compared to such fingerstick bloodsample collection by other methods or with other devices.

In embodiments of the methods disclosed herein, the time period ofcontact with the digit, or of application of pressure to the digit, is atime period that is less than the time required for the blood flow fromthe digit to slow or stop. In embodiments of the methods disclosedherein, the time period of repeated contact with the digit, or ofrepeated application of pressure to the digit, is a time period that isless than the time required for the blood flow from the digit to slow orstop. In embodiments of the methods disclosed herein, the time period ofcontact with the digit, or of application of pressure to the digit, is atime period that is less than the time required for the blood flowingfrom the digit to coagulate. In embodiments of the methods disclosedherein, the time period of cyclic pressure pulses applied to the digit,or of repeated application of pressure to the digit, is a time periodthat is less than the time required for the blood flowing from the digitto coagulate. In embodiments, such a time period of cyclic applicationof pressure pulses may be less than about 100 seconds from the time oflancing; or may be less than about 90 seconds; or may be less than about80 seconds; or may be less than about 70 seconds; or may be less thanabout 60 seconds.

In embodiments of the methods disclosed herein, the time period ofcontact with the digit, or of application of pressure to the digit, is atime period that is less than the time required for interstitial fluidin the digit to significantly contaminate the blood flowing from thedigit. In embodiments of the methods disclosed herein, the time periodof repeated contact with the digit, or of repeated application ofpressure to the digit, is a time period that is less than the timerequired for interstitial fluid in the digit to significantlycontaminate the blood flowing from the digit. In embodiments of themethods disclosed herein, significant contamination of the blood iscontamination by greater than 20% by volume interstitial fluid; or iscontamination by greater than 15% by volume interstitial fluid; or iscontamination by greater than 10% by volume interstitial fluid; or iscontamination by greater than 5% by volume interstitial fluid; or iscontamination by greater than 4% by volume interstitial fluid; or iscontamination by greater than 3% by volume interstitial fluid; or iscontamination by greater than 2% by volume interstitial fluid; or iscontamination by greater than 1% by volume interstitial fluid. Inembodiments, the time required for interstitial fluid in the digit tosignificantly contaminate the blood flowing from a digit may be greaterthan about 60 seconds from the time of lancing; or may be greater thanabout 70 seconds; or may be greater than about 80 seconds; or may begreater than about 90 seconds; or may be greater than about 100 seconds.

In embodiments of the methods disclosed herein, such time periods aretimes less than the time required for significant degradation in thequality of the sample, are times less than time required for significantdegradation of the integrity of the sample, and are times less than thetime required for loss of integrity of the sample. Indications of thedegradation in, or loss of, integrity of a sample include hemolysis ofcells in the sample, coagulation of the sample, and contamination of theblood sample by interstitial fluid.

In such embodiments, the repeated contact with, or repeated applicationof pressure to, the digit may be effective to improve the collection ofblood from the digit of the subject. In such embodiments, the pulseapplied by a device or system disclosed herein provides repeated contactwith, or repeated application of pressure to, the digit, and may beeffective to express blood from the digit of the subject.

Methods for collecting blood from a digit as disclosed herein may bepracticed or performed at any suitable location. In embodiments, such asuitable location may include a clinical laboratory, a hospital, adoctor's office, a clinic, a retail store, a school, a community center,a library, and combinations thereof. In embodiments, devices forcollecting blood from a digit as disclosed herein are located at apoint-of-care location. In embodiments, such a point-of-care location isselected from the group of point-of-care locations consisting of ahospital, a doctor's office, a clinic, and combinations thereof.

Devices and systems for automated fingerstick blood collection asdisclosed herein may provide automated pressure application to a digitof a subject; such pressure application may be sustained during acontinuous period of time. For example, a cuff 40 disposed on a digitmay be inflated, and inflation maintained for a period of time (e.g.,about 3 seconds, or about 5 seconds, or longer) prior to lancing thedigit. A period of maintained pressure prior to lancing may be termed an“initial period” of pressure application. In embodiments, pressure isapplied to the digit (e.g., the cuff is inflated) for about 3 seconds,and a signal is provided to indicate that lancing of the digit is to beperformed; such a period of time during which lancing is to be performedmay be termed a “lancing period.” Application of pressure to the digitmay be maintained during this lancing period; for example, cuff pressuremay be maintained for about 5 seconds following the initial (e.g., 3second) period of pressure application. In embodiments, pulsing (e.g.,cyclic application and relief of cuff pressure) may begin immediatelyfollowing the lancing period. Such maintained inflation may continue tobe maintained for a period of time following lancing of the digit, andmay be maintained while blood is collected from that digit.

In embodiments, such inflation may continue to be maintained for part,or for all, of the period of time following lancing while blood iscollected from that digit. Application of pressure is indicated in FIGS.4A to 4B by a horizontal line above the text and arrows of thesefigures. The “Inflate Cuff” step shown in FIGS. 4A to 4D indicates thatpressure is applied to the digit (e.g., the cuff is inflated); suchinflation of the cuff may be maintained from that time forward until the“Remove Cuff” step. The dashed portion of the horizontal line of FIG. 4Aindicates that pressure may optionally be relieved during part or all ofthe collection period; typically, when relieved in this way, pressureapplication (e.g., cuff inflation) may be relieved some time aftercollection of blood has begun. For example, in embodiments, cuffinflation may be relieved about 30 seconds, or about 40 seconds, orabout 50 seconds after collection of blood from a lanced digit hasbegun.

In addition, as shown in FIGS. 4B to 4D, such pressure application(e.g., cuff inflation) may be applied in a pulsatile manner, so that thedigit experiences periods of pressure application separated by periodsof relief of pressure (e.g., periods of cuff inflation separated byperiods of cuff deflation). Thus, the “Pulse” step indicates that thecuff inflation begun with the “Inflate Cuff” step is modulated beginningwith the “Pulse” step of FIG. 4B; pulsing the cuff may occur whilecollecting blood. Pulsing of pressure application is indicated by thediagonal lines above the steps labelled “Collect” and “Pulse” in FIGS.4B, 4C, and 4D. As indicated by the methods disclosed in FIG. 4A,methods disclosed herein may be performed with maintained pressureapplication (which is begun as indicated in FIGS. 4A to 4D by the“Inflate Cuff” step, and which then may continue until the “Remove Cuff”step) and without a “pulse” step. The methods disclosed in FIGS. 4B to4D include a “pulse” step indicating cyclic application of pressure to adigit (e.g., cyclic inflation of a cuff enclosing a digit). Such cyclicapplication of pressure may begin immediately following lancing of thedigit and initiation of blood collection, or may begin at some latertime following lancing of the digit and initiation of blood collection.

As shown in FIGS. 4A-4D, devices and systems for automated fingerstickblood collection as disclosed herein may provide automated pressureapplication to a digit of a subject (FIG. 4A); may provide automatedcyclic pressure application to a digit of a subject (FIG. 4B); and mayprovide heat application and automated cyclic pressure application to adigit of a subject (FIGS. 4C and 4D). In embodiments, lancing of thedigit may be performed manually; and in embodiments, lancing of thedigit may automated.

In particular, FIG. 4A provides a schematic diagram of methods whichautomate much of the process of obtaining blood from a subject byfingerstick. Blood may be collected by fingerstick following applicationof pressure to a digit via a cuff placed around a digit, and lancing ofthe digit. The cuff is typically positioned effective to leave aportion, typically a distal portion, of the digit exposed and availablefor lancing. The application of pressure in a cuff around a digit isbelieved to constrict the digit, and to improve the collection of bloodfrom a fingerstick, as compared to collection of fingerstick blood froma digit which is not constricted by a cuff or other means. It will beunderstood that a cuff may partially encircle, or may completelyencircle, a portion of a digit, effective to constrict a portion of thedigit when inflated. Such methods including application of pressure to aportion of a digit within a cuff, effective to constrict the digit, aredisclosed herein.

FIGS. 4B-4D disclose that pressure application may be pulsed, i.e.,pressure may be applied, released, and applied again, and may berepeatedly applied, released, and applied again. Where pressure isapplied by a cuff, a pulse may include inflation of a cuff, followed bydeflation of the cuff; and may be repeated cycles of inflation of acuff, followed by deflation of the cuff. In embodiments, deflation maybe partial deflation of a cuff. It will be understood that, inembodiments, pressure may be applied to a digit, and maintained duringcollection of blood; or may applied to a digit, and maintained for aportion of the time during collection of blood, and then pressure may bereleased for the duration of the collection time.

The application of pressure to a digit via a cuff placed around a digitis believed to impede or block blood flow out of the digit (whileallowing some blood flow into the digit), allowing blood to pool indistal portions of the digit, providing greater amounts of blood readilyavailable for collection from that digit following lancing. For examplea cuff may be placed around a finger at a position spaced away from thefingertip, and typically closer to the base of the finger than the tipof the finger. Inflation of a cuff situated in that way prevents bloodflow out of the digit tip, and prevents blood flow from the digit intothe main part of the hand. It is believed that, while the cuff isinflated, blood collects in the portion of the finger that is closer tothe finger tip than cuff. Lancing the finger, and collecting bloodflowing out of the finger, provides blood for a fingerstick bloodsample. It will be understood that, although the exemplary digitreferred to in this discussion was a finger, a fingerstick blood samplemay be obtained by the same or similar methods from a toe, or a heel, oran earlobe, or other body part or body surface.

In embodiments, a cuff may be inflated to an internal pressure of up toabout 400 millimeters of mercury (mm Hg), where such a pressure ismeasured with respect to, and is in addition to, ambient atmosphericpressure (normal atmospheric pressure is typically about 760 mm Hg).Thus, as discussed herein, where an internal pressure is indicated, suchan internal pressure is to be understood as referring to pressure thatis in addition to ambient atmospheric pressure. In embodiments, a cuffmay be inflated to an internal pressure of no more than about 400 mm Hg.In embodiments, a cuff may be inflated to an internal pressure ofbetween about 200 mm Hg and about 400 mm Hg. In embodiments, a cuff maybe inflated to an internal pressure of between about 250 mm Hg and about350 mm Hg. In embodiments, a cuff may be inflated to an internalpressure of up to about 300 millimeters of mercury (mm Hg). Inembodiments, a cuff may be inflated to an internal pressure of no morethan about 300 mm Hg. In embodiments, a cuff may be inflated to aninternal pressure of between about 200 mm Hg and about 300 mm Hg.

In embodiments, a cuff may be deflated, following inflation, to aninternal pressure of less than about 200 mm Hg. In embodiments, a cuffmay be deflated, following inflation, to an internal pressure of lessthan about 100 mm Hg. In embodiments, a cuff may be deflated, followinginflation, to an internal pressure of about 0 mm Hg. In embodiments, acuff may be deflated, following inflation, to an internal pressure ofbetween about 100 mm Hg and about 200 mm Hg. In embodiments, a cuff maybe deflated, following inflation, to an internal pressure of betweenabout 0 mm Hg and about 100 mm Hg. In embodiments, a cuff may bedeflated, following inflation, to an internal pressure of about 50 mm Hgor less. As indicated above, an internal pressure of about 0 mm Hg is aninternal pressure that does not differ from ambient atmosphericpressure.

For example, pressure application may continue for the part or all ofthe duration of the period of time during which blood is collected fromthe lanced finger. The duration of the period of time during which bloodis collected from the lanced finger may be about 20 seconds, or may beabout 30 seconds, or may be about 40 seconds, or may be about 50seconds, or may be about 60 seconds, or may be about 70 seconds, or maybe about 80 seconds, or may be about 90 seconds. In embodiments,pressure application may continue for the entire duration of the periodof time during which blood is collected from the lanced finger. Inembodiments, pressure application may continue for less than theduration of the period of time during which blood is collected from thelanced finger; for example, pressure may be released following aninitial period of time during which pressure is applied, whilefingerstick blood may be collected both during and after application ofpressure by the cuff. The duration of the period of time during whichpressure is applied, prior to releasing pressure while blood is beingcollected from the lanced finger may be about 20 seconds, or may beabout 30 seconds, or may be about 40 seconds, or may be about 50seconds, or may be about 60 seconds, or may be about 70 seconds, or maybe about 80 seconds, or may be about 90 seconds.

In embodiments, an automated device as disclosed herein may provide asignal indicating the beginning of the period of time during which bloodis to be collected from the lanced finger. Such a signal is detectableby a technician operating a device as disclosed herein, or collecting afingerstick sample of blood, or both. In embodiments, such a signal maybe a signal may be detectable without interfering with the operation ofa device as disclosed herein, or the collection of a fingerstick sampleof blood, or both, by a technician. Such a signal may be an audiblesignal (i.e., a signal which may be heard by a technician collectingfingerstick blood sample from the digit, such as the onset of a tone, orbeep, or other sound), a visible signal (i.e., a signal which may beseen by a technician collecting fingerstick blood sample from the digit,such as the onset of a light), may be a tactile signal (i.e., a signalwhich may be felt by a technician collecting fingerstick blood samplefrom the digit, such as a vibration), and may include combinationsthereof. In embodiments in which the automated device collectsfingerstick blood from a digit, the device may initiate such bloodcollection. In embodiments in which the automated device collectsfingerstick blood from a digit, the device may provide a signalindicating the beginning of the period of time during which blood is tobe collected from the lanced finger, and may initiate such bloodcollection.

In embodiments, an automated device as disclosed herein may provide asignal indicating the end of the period of time during which blood is tobe collected from the lanced finger. Such a signal is detectable by atechnician operating a device as disclosed herein, or collecting afingerstick sample of blood, or both. In embodiments, such a signal maybe a signal may be detectable without interfering with the operation ofa device as disclosed herein, or the collection of a fingerstick sampleof blood, or both, by a technician. Such a signal may be an audiblesignal (i.e., a signal which may be heard by a technician collectingfingerstick blood sample from the digit, such as the onset of a tone, orbeep, or other sound), or a visible signal (i.e., a signal which may beseen by a technician collecting fingerstick blood sample from the digit,such as the onset of a light), or may be a tactile signal (i.e., asignal which may be felt by a technician collecting fingerstick bloodsample from the digit, such as a vibration), or may include combinationsthereof. In embodiments in which the automated device collectsfingerstick blood from a digit, the device may stop such bloodcollection. In embodiments in which the automated device collectsfingerstick blood from a digit, the device may provide a signalindicating the end of the period of time during which blood is to becollected from the lanced finger, and may stop such blood collection.

FIG. 4B is a schematic diagram showing processes provided by the devicesand systems disclosed herein, effective to automate much of the processof obtaining blood from a subject by fingerstick. Blood may be collectedby fingerstick following application of pressure to a digit via a cuffplaced around a digit, lancing of the digit, and pulsing the pressureapplied by the cuff. As used herein, “pulsing the pressure” refers toinflation of the cuff followed by deflation of the cuff, and, inembodiments of “pulsing the pressure”, refers to repeated cycles ofinflation of the cuff followed by deflation of the cuff. Deflation of acuff during a pulse may be partial deflation (i.e., some residual amountof pressure remains within the cuff, where pressure is determined withrespect to ambient atmospheric pressure) or may be complete deflation(substantially no pressure remains within the cuff). The cuff istypically positioned effective to leave a portion, typically a distalportion, of the digit exposed and available for lancing. It will beunderstood that a cuff may partially encircle, or may completelyencircle, a portion of a digit, effective to constrict a portion of thedigit when inflated.

In embodiments, a cuff may be pulsed (i.e., inflated and then deflated),where when inflated the cuff is inflated to an internal pressure betweenabout 250 mm Hg and about 350 mm Hg, and when deflated the internalpressure of the cuff is reduced to about 200 mm Hg or less. Inembodiments, a cuff may be pulsed, where when inflated the cuff isinflated to an internal pressure about 300 mm Hg, and when deflated theinternal pressure of the cuff is reduced to about 100 mm Hg or less. Inembodiments, a cuff may be pulsed, where when inflated the cuff isinflated to an internal pressure about 300 mm Hg, and when deflated theinternal pressure of the cuff is reduced to about 50 mm Hg or less.

The pulsing of pressure in a cuff around a digit is believed to improvethe collection of blood from a fingerstick, as compared to collection offingerstick blood from a digit in a cuff which is not pulsed in a cyclicmanner. Such methods including cyclic pulsing of pressure within a cuff,effective to constrict and to release constriction of a digit, aredisclosed herein.

In particular, FIG. 4B provides a schematic diagram of methods whichautomate much of the process of obtaining blood from a subject byfingerstick. In the methods illustrated in FIG. 4B, fingerstick bloodmay be collected following a) application of pressure to a digit via acuff placed around a digit, b) following lancing of the digit, and c)during cyclic application of pressure to a digit via a cuff placedaround a digit. In these methods, a cuff is placed around a portion of adigit, leaving part of the digit exposed and available for lancing.Next, pressure is applied to the cuff, constricting the digit. Theapplication of pressure to a digit via a cuff placed around a digit isbelieved to impede or block blood flow out of the digit, allowing bloodto pool in distal portions of the digit, providing greater amounts ofblood readily available for collection from that digit followinglancing. Next, the digit is lanced, allowing blood to flow out of thedigit and allowing collection of the fingerstick blood sample.Collection may begin at this time. The cuff is cyclically inflated anddeflated during collection of the fingerstick blood sample. The cyclicinflation and deflation of the cuff cyclically constricts and diminishes(or releases) constriction of the digit during collection of thefingerstick blood sample. Reducing, or releasing, the pressure on thecuff may allow more blood to flow into the fingertip and to providefurther blood for a fingerstick blood sample. The cycle of pressureapplication and release of pressure may be repeated once, twice, threetimes, four times, or more times. The cycle of pressure application andrelease of pressure may be repeated multiple times, and may continue forthe duration of the period of time during which blood is collected fromthe lanced finger. It will be understood that, although the exemplarydigit referred to in this discussion was a finger, a fingerstick bloodsample may be obtained by the same or similar methods from a toe, or aheel, or an earlobe, or other body part or body surface.

For example, cyclic pressure application and release of pressure may beperformed with one second of application of pressure followed by onesecond of release of pressure; and may be repeated once, twice, threetimes, four times, or more times. For example, a cycle of pressureapplication and release of pressure, in which pressure is applied forone second, and pressure is released for one second, may be 10 times, ormay be repeated 20 times, or may be repeated 30 times, or may berepeated 40 times, or may be repeated 50 times, or may be repeated 60times, or may be repeated 70 times, or may be repeated 80 times, or maybe repeated 90 times, or more. Such a cycle may be repeated multipletimes, and may continue for the duration of the period of time duringwhich blood is collected from the lanced finger. In embodiments in whichpressure is cyclically applied to a digit by a cuff, the duration of theperiod of time during which blood is collected from the lanced fingermay be 10 seconds, 20 seconds, 30 seconds, 40 seconds, 50 seconds, 60seconds, 70 seconds, 80 seconds, 90 seconds, or more. In embodiments inwhich pressure is cyclically applied to a digit by a cuff, the durationof the period of time during which blood is collected from the lancedfinger may be about 50 seconds, or may be about 60 seconds, or may beabout 70 seconds, or may be about 80 seconds, or may be about 90seconds.

In embodiments, as discussed above, an automated device as disclosedherein may provide a signal indicating the beginning of the period oftime during which blood is to be collected from the lanced finger. Asdiscussed above, such a signal may be an audible signal, a visiblesignal, may be a tactile signal, and may include combinations thereof.In embodiments in which the automated device collects fingerstick bloodfrom a digit, the device may initiate such blood collection. Inembodiments in which the automated device collects fingerstick bloodfrom a digit, the device may provide a signal indicating the beginningof the period of time during which blood is to be collected from thelanced finger, and may initiate such blood collection.

In embodiments, an automated device as disclosed herein may provide asignal indicating the end of the period of time during which blood is tobe collected from the lanced finger. Such a signal may be an audiblesignal (i.e., a signal which may be heard by a technician collectingfingerstick blood sample from the digit, such as the onset of a tone, orbeep, or other sound), or a visible signal (i.e., a signal which may beseen by a technician collecting fingerstick blood sample from the digit,such as the onset of a light), or may be a tactile signal (i.e., asignal which may be felt by a technician collecting fingerstick bloodsample from the digit, such as a vibration). In embodiments in which theautomated device collects fingerstick blood from a digit, the device maystop such blood collection. In embodiments in which the automated devicecollects fingerstick blood from a digit, the device may provide a signalindicating the end of the period of time during which blood is to becollected from the lanced finger, and may stop such blood collection.

FIGS. 4C and 4D are schematic diagrams showing processes provided by thedevices and systems disclosed herein, effective to automate much of theprocess of obtaining blood from a subject by fingerstick. Inembodiments, methods as illustrated in FIGS. 4C and 4D may include stepsas indicated in FIG. 4B and further include warming a digit (e.g.,warming a digit prior to application of a cuff to a digit, as shown inFIG. 4C; and warming a digit following application of a cuff to a digit,as shown in FIG. 4D); in such embodiments, blood may be collected byfingerstick following application of pressure to a digit via a cuffplaced around a digit, warming the digit, and lancing of the digit. Inembodiments further including pulsing pressure in a cuff as illustratedin FIGS. 4C and 4D, blood may be collected by fingerstick followingapplication of pressure to a digit via a cuff placed around a digit,warming the digit, and lancing of the digit, and pulsing the pressureapplied by the cuff. Thus, methods including steps as illustrated inFIGS. 4C and 4D include warming a digit, and include steps as indicatedin FIGS. 4A and 4B, and as discussed above with regard to FIGS. 4A and4B.

In embodiments, warming a digit may begin prior to inflating a cuff inwhich the digit is placed. In embodiments, a warming mechanism may bepart of a cuff, effective to contact a digit when the cuff is placed onor around the digit. In embodiments, a warming mechanism may be within acuff, effective to warm a digit when the cuff is placed on or around thedigit. In embodiments, a warming mechanism may be disposed on anexterior surface of a cuff, effective to contact a digit for warming thedigit when the cuff is placed on or around the digit. In embodiments, awarming mechanism may be connected to a part of a cuff, effective tocontact a digit for warming the digit when the cuff is placed on oraround the digit. In embodiments, warming a digit may begin prior tolancing the digit. In embodiments, warming a digit may begin prior tolancing the digit, and may cease prior to lancing the digit. Inembodiments, warming a digit may begin prior to lancing the digit, andmay continue following lancing the digit.

Embodiments of the automated fingerstick blood collection methods,devices, systems, and kits disclosed herein include a kit forfingerstick blood collection, comprising a device as disclosed hereinand a sample collection vessel. In an embodiment, a kit for fingerstickblood collection comprises a device as disclosed herein, a samplecollection vessel, and a disposable for use in sample collection. Inembodiments, a disposable for use in sample collection may be a sterileswab (e.g., an alcohol swab), may be an absorbent pad (e.g., a cottongauze pad for placement over a fingerstick wound), may be a bandage(e.g., a small self-adhesive bandage for placement over a fingerstickwound or over a gauze pad on a fingerstick wound), other disposables foruse in a sample collection location (e.g., a clinical laboratory, adoctor's office, a clinic, a retail location, or other location in whicha fingerstick sample may be obtained from a subject), and combinationsthereof.

In embodiments, a device having features as disclosed herein isconfigured to provide automated finger-pressure cycling and to indicatea collection period (a “collection window”) that is a fixed period oftime. In embodiments, a device having features as disclosed herein isconfigured to provide automated finger-pressure cycling, to indicate acollection period (a “collection window”) that is a fixed period oftime, and includes a finger warmer. In embodiments, a device havingfeatures as disclosed herein is configured to provide automatedfinger-pressure cycling, to indicate a collection period (a “collectionwindow”) that is a fixed period of time, includes a finger warmer, andincludes an integrated finger-lancing element.

In embodiments, a system having features as disclosed herein isconfigured to provide automated finger-pressure cycling and to indicatea collection period (a “collection window”) that is a fixed period oftime. In embodiments, a system having features as disclosed herein isconfigured to provide automated finger-pressure cycling, to indicate acollection period (a “collection window”) that is a fixed period oftime, and includes a finger warmer. In embodiments, a system havingfeatures as disclosed herein is configured to provide automatedfinger-pressure cycling, to indicate a collection period (a “collectionwindow”) that is a fixed period of time, includes a finger warmer, andincludes an integrated finger-lancing element.

FIG. 5 shows housings and portions of conduits and power connections ofdevices having features as disclosed herein, providing examples ofindicator lights in different configurations. Individual configurationsare indicated by illumination of indicator lights. The left-mostindicator light of the device depicted on the left of the figure isshown illuminated to indicate that pressure is being applied by thedevice to a finger of a subject. The central indicator light of thedevice depicted in the middle of the figure is shown illuminated toindicate that a lancet is to be applied to a finger of a subject toprovide a fingerstick wound for obtaining blood from the subject. Theright-most indicator light of the device depicted on the right of thefigure is shown illuminated to indicate that blood may be collected fromthe fingerstick wound of the finger of the subject.

FIG. 6 shows housings and portions of conduits and power connectionsdevices having features as disclosed herein. The figures show indicatorlights for alerting a user of the occurrence of an error. FIG. 6 showsindicator lights lit in each of two configurations. Individualconfigurations are indicated by illumination of indicator lights. Theleft error indicator light of the device depicted on the device on theleft portion of the figure is shown illuminated to indicate that anerror condition has occurred related to the pressure cuff. The righterror indicator light of the device depicted on the right portion of thefigure is shown illuminated to indicate that an error condition hasoccurred related to the foot pedal (which is used to interrupt thesequence of pressure pulses in the cuff).

FIG. 7A provides a schematic diagram detailing steps for obtaining afingerstick blood sample according to methods of using the devices andsystems disclosed herein. The figure explicitly names the digit as afinger, although a fingerstick blood sample may be obtained from a toe,or other body surface. As illustrated in FIG. 7A, a cuff is placed on adigit (e.g., a finger), and the start button is pressed, initiatinginflation of the cuff. Inflation of the cuff constricts the digit andoccludes blood flow in the digit, preparing it for collection of afingerstick blood sample. Proper placement of the cuff leaves at leastabout 5 mm of skin surface of the digit exposed following inflation ofthe cuff; for example, at least about 5 mm of the distal (tip) portionof a digit such as a finger or toe may be left exposed while the cuff isin place and is inflated. A cuff of the devices and systems disclosedherein is sized so as to provide sufficient exposed skin surface wheninflated and disposed in place on a digit. A signal (e.g., an audiblesignal, such as a beep, as indicated in FIG. 7A) is provided by thedevice to alert a user that constriction by the cuff has proceeded for asufficient amount of time, and that the digit may be lanced. The digitis lanced, and a further signal indicates that collection of blood mayproceed. Blood is collected from the wound site, and, a further alert(e.g., a further audible signal) is provided at the end of the period oftime during which a high quality fingerstick blood sample may becollected. The alert signals the end of the collection period. Bloodcollection ends at this time (if blood collection was still proceeding;in many cases, sufficient amount of blood is collected prior to reachingthe end of the collection period).

If a sufficient amount of blood was collected by, or prior to, the endof the collection period (as indicated by the question “Vessel Filled?”in FIG. 7A), the sample is placed in a storage container or location, oris placed in a transport container, or is provided to a sample analysisdevice or system for analysis. Gauze, bandage, or other treatment may beplaced on, or applied to, the digit. The cuff is deflated, and may beremoved from the digit.

If, however, an insufficient amount of blood was collected by, or priorto, the end of the collection period, a further sample, typicallyobtained from a different digit, may be obtained, by beginning the stepsagain from the beginning. If a portion of the desired amount is still ofuse, then that portion may be placed in a storage container or location,or is placed in a transport container, or is provided to a sampleanalysis device or system for analysis. If a too-small amount of bloodmakes the desired analysis impossible, then the sample may be discarded.

FIG. 7B provides a schematic diagram detailing steps of obtaining afingerstick blood sample according to methods of using the devices andsystems disclosed herein, in which a digit (e.g., a finger) is warmedprior to placing a cuff on the digit. These steps are identical to thoseshown in FIG. 7A, with the difference that the steps of FIG. 7B furtherinclude a step of warming the digit prior to beginning fingerstick bloodcollection. A digit may be warmed for at least about 45 seconds prior tosample collection, and may be warmed for about 50 seconds, or about 60seconds, or about 70 seconds, or about 80 seconds, or more. Warming adigit prior to sample collection may begin prior to placement of thecuff on the finger (e.g., as shown in FIG. 7B), or may begin withplacement of the cuff on the digit, or may begin following placement ofthe cuff on the digit. Warming typically begins prior to inflation ofthe cuff on the digit. As indicated, for example, in FIG. 2B, a cuff mayinclude a warming mechanism, which may be activated effective to warm adigit when the cuff is placed on the digit. In embodiments, a warmingmechanism may be separate from a cuff; such a warming mechanism may beapplied prior to, or during, placement of the cuff on the digit, orwhile the cuff is in place on the digit. In embodiments, a separatewarming mechanism may be applied to a digit and a warming mechanism in acuff may be activated (e.g., while the cuff is in place on the digit).In embodiments, a separate warming mechanism may be applied to a digitprior to placement of a cuff on the digit, and a warming mechanism in acuff may be activated after the cuff is in place on the digit.

An interrupt switch 36 may be configured to be operated with minimalinterference with collection of a fingerstick blood sample; for examplean interrupt switch 36 may be a foot pedal, which a technician mayoperate at the same time that technician is collecting blood from asubject without requiring the use of a hand to interrupt pressureapplication. An interrupt switch 36 configured to interrupt pressureapplication is optional; some embodiments of the devices disclosedherein may lack an interrupt switch 36.

As discussed above, an interrupt switch (e.g., an interrupt switch 36 asshown in FIGS. 2A-2E and in 3A and 3B) may interrupt pressureapplication, or allow pressure release, or both, effective to interruptthe inflation of a cuff while the interrupt switch is activated. Inembodiments, activation of an interrupt switch pauses the pressurecycling of the cuff to allow blood flow rate control. In embodiments, aninterrupt switch may be a foot pedal, and pressing the foot pedal maypause the pressure cycling of the cuff to allow blood flow rate control.Activation of an interrupt switch provides a temporary pause ininflation of a cuff; typically, where a sample collection vessel isfilled before the end of the full time period for collection of afingerstick blood sample, the “stop” button may be pressed to end thecollection program.

The devices and systems disclosed herein may be operated by a technicianfor use on a patient to collect a sample of blood from the patient. Inembodiments, use of the devices and systems disclosed herein forobtaining a blood sample from a patient are simple to use, and, in use,cause only minimal discomfort to a patient. In embodiments, a technician(user) may easily and readily use the devices and systems disclosedherein with minimal training. Some types of users of the devices andsystems disclosed herein are discussed in the following.

In embodiments, users of devices and systems disclosed herein will betrained on the device use prior to operating the product. Users of thedevices and systems disclosed herein include phlebotomists, technicians,and trainers. Phlebotomists may be certified by an appropriatecertification entity.

Trainers: Trainers are personnel who are thoroughly trained and educatedon the Fingerstick Blood Collection Process. Trainers are capable oftraining Technicians and Phlebotomists in the field. Trainers willtypically have a minimum of a college degree, which need not be in atechnical field.

Phlebotomists: Phlebotomists will typically have training and experiencewith fingerstick and/or heel stick blood collection methods. In mostcases, however, the primary focus of phlebotomy training programs isvenous-based blood collection, so that phlebotomists may benefit fromfocused training, such as may be available from trainers. Certifiedphlebotomists are required to have a minimum of a high school diploma asa prerequisite to any phlebotomy certification program.

Technicians: Technicians may have little or no prior experience with anytype of blood collection or patient interaction, and may not necessarilyhave a high school diploma. Technicians should receive training onfingerstick blood collection methods and techniques prior to using thedevices and systems, and prior to practicing the methods, disclosedherein.

In embodiments, only a minimal amount of training is required to train atechnician in the operation and use of a device or system forautomatically providing cycling pressure application to a digit of asubject. In embodiments, a minimal amount of training is only about 30minutes of training, or may be less than about 30 minutes of training,in order that a technician receive sufficient training to be able toproperly and safely operate the devices and systems, and to properly andsafely collect fingerstick samples from subjects.

Devices and systems disclosed herein are designed to directly replacemanual pressure cycling of the patient's finger during fingerstick bloodcollection. Thus, use of the methods, devices, systems, and kitsdisclosed herein will obviate any need to manually manipulate asubject's extremity during fingerstick blood collection.

In embodiments, devices and systems disclosed herein will typically beoperated in indoor environments where electricity is available. Inembodiments, devices and systems disclosed herein may be used on adultsubjects, and in embodiments, may be used on pediatric subjects, such aschildren and infants.

In embodiments, the devices for automatically providing cycling pressureapplication to a digit of a subject are table-top devices (i.e., devicesof small enough size to fit on a normal table during use). Inembodiments, systems including a device for automatically providingcycling pressure application to a digit of a subject are table topsystems. In embodiments, a table-top device or system will have ahousing with a largest dimension that is smaller than about three feet,or is smaller than about two feet, or is smaller than about 1 foot insize. In embodiments, a table-top device or system will have a housingthat weighs less than about 30 pounds, or less than about 20 pounds, orless than about 10 pounds.

In embodiments, the devices for automatically providing cycling pressureapplication to a digit of a subject integrate into the existingenvironment and workflow of a clinical laboratory, physician's office,retail location, or other location where fingerstick samples may becollected. In embodiments, systems including a device for automaticallyproviding cycling pressure application to a digit of a subject integrateinto the existing environment and workflow of a clinical laboratory,physician's office, retail location, or other location where fingersticksamples may be collected.

Kits

In embodiments, kits for collecting blood from a digit are disclosedherein. In embodiments, kits for collecting blood from a digit include adevice as disclosed herein, and a sample collection vessel. Inembodiments, kits for collecting blood from a digit comprise a device asdisclosed herein, a sample collection vessel, and a disposable for usein sample collection. In embodiments, kits for collecting blood from adigit comprise a device as disclosed herein, a sample collection vessel,a lancet for puncturing a digit, and a disposable for use in samplecollection. In embodiments, kits for collecting blood from a digitcomprise a disposable selected from the group of disposables consistingof a swab, a sterile swab, an absorbent pad, and a bandage.

Applicant discloses herein kits including devices or systems asdisclosed herein, and further including a sample collection device orsample collection vessel suitable for collecting a fingerstick bloodsample. Applicant discloses herein kits including devices or systems asdisclosed herein, and further including a sample transport vesselsuitable for transporting a fingerstick blood sample from a site ofcollection to another location (e.g., to a laboratory location). Samplecollection devices and vessels are disclosed, for example, in U.S.patent application Ser. No. 14/020,435, filed Sep. 6, 2013; U.S. patentapplication Ser. No. 14/098,177, filed Dec. 5, 2013; U.S. patentapplication Ser. No. 14/214,774, filed Mar. 15, 2014; U.S. patentapplication Ser. No. 14/320,471, filed Jun. 30, 2014; U.S. patentapplication Ser. No. 14/446,080, filed Jul. 29, 2014; and U.S. patentapplication Ser. No. 14/447,099, filed Jul. 30, 2014, the entirecontents of which patent applications are hereby incorporated byreference in their entireties for all purposes.

Kits disclosed herein may include devices or systems as disclosedherein, and further include a disposable useful in or after collecting afingerstick blood sample; for example a disposable may be a lancet(which may be, e.g., a blade or a needle), such as a manually operatedlancet, a spring-operated lancet, a lancet having a sheath, or otherlancet. Kits disclosed herein may include devices or systems asdisclosed herein, and further include a disposable for use in collectinga fingerstick blood sample, where, for example the disposable is abandage, a gauze pad, an absorbent pad, a swab, a sterile swab, or otherdisposable. Kits disclosed herein may include devices or systems asdisclosed herein, and further include a disposable for use in collectinga fingerstick blood sample, where, for example the disposable is alabel, such as, e.g., a bar-code label, or a QR code label, or otherlabel.

Uses

The methods, devices, and systems disclosed herein may be used to obtainblood samples from subjects, including adult (standard cuff), pediatric(smaller cuff), geriatric (typically standard cuff), and other subjects.Blood samples may be obtained from a digit of a subject, e.g., from afinger or fingers of a subject. In embodiments, blood samples may beobtained from a toe or toes of a subject. The methods, devices, andsystems disclosed herein may be used to obtain blood samples forclinical use, e.g., for clinical diagnostic use. Clinical uses mayinclude routine clinical testing, esoteric clinical testing, screeningfor the presence of drugs or drug metabolites; screening for thepresence or absence of disease markers; screening for the presence orabsence of genetic markers; paternity testing; determination ofancestry; and for other reasons and purposes.

In embodiments, the methods, devices, and systems disclosed herein maybe used to obtain blood samples for research use. In embodiments, themethods, devices, and systems disclosed herein may be used to obtainblood samples for use by insurance companies in determining thesuitability of insurance coverage, or the cost of insurance coverage,for a subject; for identification of a subject; for administrativepurposes; for archival purposes; and for any other purpose for which ablood sample may be obtained.

Devices for collecting blood from a digit as disclosed herein may belocated any suitable location. In embodiments, such a suitable locationmay include a clinical laboratory, a hospital, a doctor's office, aclinic, a retail store, a school, a community center, a library, andcombinations thereof. In embodiments, devices for collecting blood froma digit as disclosed herein are located at a point-of-care location. Inembodiments, such a point-of-care location is selected from the group ofpoint-of-care locations consisting of a hospital, a doctor's office, aclinic, and combinations thereof.

Systems for collecting blood from a digit as disclosed herein may belocated any suitable location. In embodiments, such a suitable locationmay include a clinical laboratory, a hospital, a doctor's office, aclinic, a retail store, a school, a community center, a library, andcombinations thereof. In embodiments, devices for collecting blood froma digit as disclosed herein are located at a point-of-care location. Inembodiments, such a point-of-care location is selected from the group ofpoint-of-care locations consisting of a hospital, a doctor's office, aclinic, and combinations thereof.

Examples

Exemplary methods for using the devices and systems disclosed herein arediscussed in the following. In the following, reference is made to thedevice; it will be understood that such references apply with equalforce to systems as disclosed herein, which systems include suchdevices. The user of the devices and systems disclosed herein is termeda “technician” in the following examples; it will be understood thatthis technician may be any user capable of operating the devices andsystems during fingerstick blood sample collection as disclosed herein.In the following examples, the digit from which a fingerstick bloodsample is collected is termed a “finger”; however, it will be understoodthat any digit, including a toe, or other skin surface (e.g., a heel, orearlobe) may be used to collect a fingerstick blood sample. In thefollowing, the subject from whom the fingerstick blood sample iscollected is identified as the “patient”; however, it will be understoodthat any person, whether a patient suffering from a disease, or beingmonitored for a medical condition, or undergoing for routine medicaltesting, or a research subject, or other subject, may be the source of afingerstick blood sample.

Performance Features and Characteristics for Normal Operation

Devices and systems for collection of fingerstick blood samples aredisclosed herein. Devices having features as disclosed herein may beused in, and make up part of, systems having features as disclosedherein. Methods for the use of these devices and systems for collectingfingerstick blood samples are disclosed herein. Operation of thesedevices and systems may be performed according to such methods; inembodiments, operation of these devices and systems may be according toa program. Such a program may include automatic steps, including apre-determined order of steps, which govern the operation of a device orsystem as disclosed herein. In embodiments, as used in the following,the term “the program” refers to a process that includes many or allsteps for collection of a fingerstick blood sample using a device orusing a system disclosed herein. Devices may include a processor, andmay include memory (e.g., digital memory, such as read-only memory,random access memory, flash memory, or other memory, or combinationsthereof). Such memory may be effective to store a program for operationof a device as disclosed herein. A processor, or a processor and memory,may be effective to control the operation of a device as disclosedherein. Devices and systems may further include a timing mechanism(e.g., a timer such as a timing chip, a mechanical timer, or othertimer), which may be operably configured for use with a processor, orfor use with a processor and memory, effective to control the operationof a device as disclosed herein according to times and time periods asneeded for the operation of a device for collecting fingerstick bloodsamples.

In embodiments, devices as disclosed herein may include a housing. Inembodiments, such a housing may enclose a processor. In embodiments,such a housing may enclose digital memory, or other form of electronicmemory. In embodiments, such a housing may enclose a timing mechanism.In embodiments, such a housing may enclose a pressure source. Inembodiments, such a housing may enclose a power supply, or a battery, orother elements for providing power to other components of the device orfor converting power to a suitable form or use by other components ofthe device. A housing may have a switch, such as an ON/OFF switch, andmay have a plurality of switches, each of which may be accessible foruse by a user of the device. A housing may have an indicator, such as anindicator light, visible to a user of the device, or otherwise capableof providing an indication to a user of the device. A housing may have aplurality of indicators. A housing may have a sound generator, such as abeeper, speaker, or bell, and may have a plurality of sound generators,each of which may be audible by a user of the device when activated. Ahousing may have a connector configured to receive and hold a conduit;in embodiments, such a connector may be configured to provide pressurefrom a pressure source to a conduit. In embodiments, such a conduit mayinclude a cuff, or may be configured to accept or carry a cuff, wherethe cuff is an inflatable cuff configured for placement on a digit.

Devices having features as disclosed herein may be designed andconfigured to provide the following outputs and performancecharacteristics.

These devices may be configured to apply pressure to the circumferenceof the patient's finger at a repeatable distance from the fingertip. Inembodiments, such a distance is about 5 to 25 mm from the tip (or otherextreme portion of the digit). In embodiments, such a distance is about5 to 10 mm from the tip (or other extreme portion of the digit). Inembodiments, such a distance is at least about 5 mm from the tip (orother extreme portion of the digit).

These devices may be configured to use audio cues to provide feedback tothe user. In this way, the user (operator) is able to remain focused onthe patient and on the task of blood collection into the device or intoa sample collection vessel. Such device audio cues may be provided atone or more of: at the start of the program, the start of the lancingperiod, the start of the collection period, the end of the program, andfor all errors. These devices may be configured to indicate programprogress and error status to the user. These devices may have a singlebutton to start and stop the device program.

These devices may have a foot pedal which deflates the cuff while thepedal is pushed. Pressing the foot pedal does not impact the programtimer. Use of the foot pedal allows the user to control the flow rate ofblood from the finger by allowing the user to briefly interrupt cuffinflation and allow a period of cuff deflation. These devices may beconfigured to provide a tourniquet period during which the cuff isinflated for 3 seconds. Such a tourniquet period mimics manualcollection technique (i.e., techniques in which a technician manuallysqueezes a digit in order to constrict the digit and reduce or preventblood flow out of the digit). Applying a tourniquet-like grip on thefinger is thought to help to reduce the pain associated with lancing andto help collect the blood into the finger. These devices may beconfigured to have a lancing period during which the cuff remainsinflated for 5 seconds after the lancing audio cue. This mimics manualcollection technique. These devices may be configured to have acollection period during which the cuff is cyclically held inflated for1 second then deflated for 1 second for a total of 60 seconds after thelancing cue. In one non-limiting example, the collection window is a 60second collection window based on studies indicating that after 60seconds, the likelihood of collecting clotted blood samples is increasedfor some patients. In embodiments, the collection window may be a 70second collection window, or may be a 80 second collection window. Thesedevices may be configured to be capable of detecting pressure problemswith the cuff and of indicating an error. These devices may beconfigured to be capable of detecting whether the foot pedal is pluggedin and indicate an error if it is missing. These devices may beconfigured to deflate the cuff and discontinue operation if an errorstate is detected. Optionally, some embodiments may adjust the length ofthe collection window based on exogenous factors such as but not limitedto the time of the year (e.g., winter, summer, fall, or spring), currenttemperature, barometric pressure, or other factor(s) that may impact thesample collection process. This information may be communicated to thepressure application device or the device may have sensors to measuresuch exogenous factors directly.

In embodiments, use of these devices may allow collection of a 200fingerstick blood sample volume within a sample collection period ofabout 90 seconds. In embodiments, use of these devices may allowcollection of a 200 μL fingerstick blood sample volume within a samplecollection period of about 80 seconds. In embodiments, use of thesedevices may allow collection of a 200 μL fingerstick blood sample volumewithin a sample collection period of about 70 seconds. In embodiments,use of these devices may allow collection of a 200 μL fingerstick bloodsample volume within a sample collection period of about 60 seconds.

These devices may be configured to inflate a cuff to a pressure of about300 mm Hg during normal operation; in embodiments, a cuff may beinflated to a pressure of about 300 mm Hg in less than 10 seconds, or inless than 5 seconds, in less than 3 seconds, in less than 2 seconds, inless than 1 seconds. These devices may be configured to maintain thecuff inflation pressure of about 300 mmHg over a period of 10 seconds.These devices may be configured to prevent inflation of the cuff over apressure of 300 mm Hg. In embodiments, these devices may be configuredto deflate a cuff in less than 3 seconds after the stop button ispressed, in less than 2 seconds after the stop button is pressed, or inless than 1 second after the stop button is pressed.

In embodiments, a cuff of a device having features as disclosed hereinmay be disposable; use of disposable cuffs may reduce or preventpatient-to-patient contamination. In embodiments, these devices,including cuffs of these devices, may be made of materials suitable forcleaning; for example, these devices may be made of materials suitablefor wiping by isopropyl alcohol-based disinfectant wipes or by otherdisinfectant wipes.

These devices may be configured for use with subjects having digits of awide range of digit size. In embodiments, devices having features asdisclosed herein may be configured to operate with digits ranging insize from as small as the size of a finger of the smallest 1^(st)percentile of adult females up to as large as the size of a finger ofthe largest 99^(th) percentile adult males. For example, cuffs havingfeatures as disclosed herein may be configured to operate with digitsranging in size from about 1 centimeter (cm) to about 3 cm in diameter.In embodiments, cuffs having features as disclosed herein may beconfigured to operate with digits ranging in size from about 1.3 cm toabout 2.5 cm diameter.

In embodiments of devices having features as disclosed herein, cuffs maybe sized so as to allow a gap of about 5 mm or more as measured from thepatient's fingertip to the cuff to allow space for lancing the finger.In embodiments, such a gap may be a gap of about 10 mm or more. Inembodiments of methods using devices having features as disclosedherein, cuffs may be placed on a digit so as to allow a gap of about 5mm or more as measured from the patient's fingertip to the cuff to allowspace for lancing the finger. In embodiments, cuffs may be placed on adigit so as to allow a gap of about 10 mm or more. These devices may becapable of operating on the patient's left hand (or foot) or on thepatient's right hand (or foot). These devices may be configured foroperation by a left-handed or by a right-handed technician. Thesedevices may be configured for operation by a technician wearing gloves.In embodiments, these devices may be configured for use with electricalpower that is typically available from standard wall-sockets. Inembodiments, these devices may be battery powered. In embodiments, thesedevices may be powered by rechargeable batteries. In embodiments, thesedevices may be configured for use with either batteries or withelectrical power that is typically available from standard wall-sockets.Devices having features as disclosed herein are typically simple tosetup and simple to operate; in embodiments, these devices may becapable of operation within less than about 10 minutes of the initialinstallation of the device.

Normal Use Case: Collection Completed Prior to Collection WindowExpiration

In normal use in collecting a fingerstick blood sample from a subject,the following steps are taken. 1) Technician attaches a new cuff to thedevice. In embodiments, the conduit providing pressure from the housingof the device (in which the pressure source may be located) to the cuffis part of the device, and is configured to mate with a disposable cuff.In embodiments, the cuff is permanently attached to the conduitproviding pressure from the housing of the device, so that the cuff andthe conduit form a single unit which may be attached to the housing inwhich the pressure source may be located. 2) Technician places the cuffon the patient's finger and slides it back toward the palm as far aspossible to allow space for disinfecting the finger. 3) Techniciandisinfects the patient's finger with an alcohol wipe and allows it todry. 4) Technician places cuff at the indicated distance from thepatient's fingertip and supports the finger with his/her non-dominanthand. 5) Technician hits a start button on the device and picks up thelancet with his/her dominant hand. 6) The device beeps and pressurizesthe cuff to tourniquet the patient's finger for 3 seconds. 7) The devicebeeps to indicate to the Technician to lance the finger and holdspressure for 5 seconds during the lancing period. 8) The Technicianlances the patient's finger, places the lancet in a sharps container,and picks up the blood collection device and begins collecting theblood. 9) The device beeps to indicate the start of the collectionperiod and begins to cycle squeezing and releasing pressure on thepatient's finger. 10) The Technician collects the blood produced intothe collection device until the device is full. 11) The Technician hitsthe pause pedal to stop the pressurizing the finger, places thepatient's finger on the gauze, and asks the patient to apply pressure tostop any bleeding. 12) The Technician operates the blood collectiondevice, and then presses the stop button on the device to end theprogram (if the collection window has not expired). The collectionwindow is typically 60 seconds, and (optionally) may be 70 seconds or 80seconds. 13) The technician removes the cuff from the patient's fingerthen places a bandage on the finger. 14) The cuff may be detached fromthe housing of the device and disposed in the trash. In embodiments, theconduit connecting the cuff to the housing (which contains the source ofpressure) may be re-used by attaching a new cuff to the conduit for usewith a subsequent subject. In embodiments, the conduit and the cuff maybe provided as a single unit, and that unit (including the conduit andthe cuff) may be detached from the housing and discarded, and a newconduit and the cuff unit attached to the housing for use with asubsequent subject. Optionally, some embodiments may have a cuff unit orother pressure application unit that has a tear-away contact layer thatcovers any portion of the cuff unit or pressure application unit thatmay be pressing against the subject. In such a non-limiting embodiment,the tear-way portion can be replaced each time a new patient or subjectis being processed without having to completely replace the cuff unit orpressure application unit for each collection event. This may reducecosts in terms of minimizing the amount of equipment to replace for eachcollection event. In one non-limiting example, the tear-away portion mayuse an adhesive, Velcro™ connectors, hook/loop/fabric connectors, orother releasable connections for attaching a tear-away sheet, membrane,or other covering for disposal after each use. Some embodiments mayincorporate a heating element, chemical heat-pad, or the like with thedisposable cover or layer portion.

Alternative Use Case: Patient Blood Flow Rate Too High for CollectionDevice

If, in step 8 or 10 above, the blood flow from the fingerstick wound istoo high to collect into the blood collection device, then the followingmethods may be performed.

1) The technician press and holds the pause (foot) pedal which causesthe device to depressurize the finger until the pedal is released. Thisallows the technician to control the blood flow rate from the finger.Note: pressing the pause pedal does not affect the collection timer; thecollection window remains fixed.

2) Release of the pause pedal causes the device to continue pressurizingthe finger.

Alternative Use Case: Foot Pedal not Attached.

If in step 5 of the Normal Use Case, the device does not detect that thefoot pedal is connected: 1) The device will show a foot pedal error andnot start the collection program. 2) The technician plugs in the footpedal and the error resets. 3) The technician continues with step 5 ofthe Normal Use Case.

Alternative Use Case: Cuff not to Pressure

If during step 6, the device does not reach the pressure set point,then: 1) The device will show a cuff error and discontinue thecollection program. 2) The technician will check the cuff for possiblecauses of the error (e.g., cuff not attached; cuff leaking; cuff notproperly affixed around finger; or other cause). 3) The techniciancontinues with step 5 of the Normal Use Case.

While the invention has been described and illustrated with reference tocertain particular embodiments thereof, those skilled in the art willappreciate that various adaptations, changes, modifications,substitutions, deletions, or additions of procedures and protocols maybe made without departing from the spirit and scope of the invention. Byway of non-limiting example, although many embodiments herein describethe use of a pneumatic system for application of pressure, it should beunderstood that other techniques for application of pressure such as butnot limited to mechanical, electromechanical, piezoelectric, or othercurrent technologies or those to be developed in the future may be usedto apply a desired amount of pressure to a portion of the subject. Someembodiments may use at least one of linear actuators, pistons,screw-drives, worm-drives, pneumatic actuators, voice coil-typeactuators, diaphragms, or other devices to provide the desired pressure.Some embodiments may use single or multiple combinations of theforegoing to provide a desired pressure or pattern of applied pressure.Some embodiments may be configured to apply pressure to more than onedigit on the same hand. Some embodiments may be configured to applypressure to at least one digit on a first body party and a least anotherdigit on a second body part. In some embodiments, a warming pad or otherwarming component may be part of the device in contact with the subjectand may be detached, moved, or otherwise positioned to reveal a targetsite for sample collection after the target site has been sufficientlywarmed, wherein such uncovering or unveiling of the target site does notimpact the pressure application portions of the device. Optionally, someembodiments may use a non-contact warming technique such as but notlimited to an infrared heating, laser, or other non-direct contactheating technique.

Additionally, concentrations, amounts, and other numerical data may bepresented herein in a range format. It is to be understood that suchrange format is used merely for convenience and brevity and should beinterpreted flexibly to include not only the numerical values explicitlyrecited as the limits of the range, but also to include all theindividual numerical values or sub-ranges encompassed within that rangeas if each numerical value and sub-range is explicitly recited. Forexample, a size range of about 1 nm to about 200 nm should beinterpreted to include not only the explicitly recited limits of about 1nm and about 200 nm, but also to include individual sizes such as 2 nm,3 nm, 4 nm, and sub-ranges such as 10 nm to 50 nm, 20 nm to 100 nm, andso forth.

The publications discussed or cited herein are provided solely for theirdisclosure prior to the filing date of the present application. Nothingherein is to be construed as an admission that the present invention isnot entitled to antedate such publication by virtue of prior invention.Further, the dates of publication provided may be different from theactual publication dates which may need to be independently confirmed.All publications mentioned herein are incorporated herein by referenceto disclose and describe the structures and/or methods in connectionwith which the publications are cited.

While preferred embodiments of the present invention have been shown anddescribed herein, it will be obvious to those skilled in the art thatsuch embodiments are provided by way of example only. Numerousvariations, changes, and substitutions will now occur to those skilledin the art without departing from the invention. It should be understoodthat various alternatives to the embodiments of the invention describedherein may be employed in practicing the invention. Any feature, whetherpreferred or not, may be combined with any other feature, whetherpreferred or not. The appended claims are not to be interpreted asincluding means-plus-function limitations, unless such a limitation isexplicitly recited in a given claim using the phrase “means for.”

1. A device comprising: a cuff configured to at least partially encirclea human digit; a pressure source configured to inflate said cuffeffective to apply pressure to a digit disposed at least partiallywithin the cuff; and a timing mechanism configured to provide a timingmechanism signal at the beginning of a period of time and a timingmechanism signal at the end of said period of time, where the period oftime is a desired period of time for collecting a fingerstick bloodsample from said digit, wherein said device is configured to end theinflation of said cuff at the end of the period of time. 2-8. (canceled)9. The device of claim 1, wherein said cuff is configured to be inflatedup to a maximum pressure of about 300 millimeters (mm) of mercury (Hg)of pressure.
 10. (canceled)
 11. The device of claim 1, wherein said cufffurther comprises a warming mechanism configured to warm a digitdisposed within said cuff. 12-14. (canceled)
 15. The device of claim 1,wherein said cuff comprises a plurality of lobes, wherein each lobe maybe inflated independently of the other lobe or lobes.
 16. The device ofclaim 1, wherein said cuff forms a tubular structure configured tocompletely encircle a digit placed within the internal portion of saidstructure. 17-18. (canceled)
 19. The device of claim 1, furthercomprising a lancing mechanism configured to puncture a digit effectiveto make a wound or incision in said digit, wherein said wound issuitable for providing blood for sample collection.
 20. The device ofclaim 15, further comprising a lancing mechanism configured to puncturea digit effective to make a wound or incision in said digit, whereinsaid wound is suitable for providing blood for sample collection. 21.The device of claim 1, further comprising a pressure-interruptionswitch.
 22. (canceled)
 23. The device of claim 1, further comprising acommunication unit configured to transmit data selected from the groupof data consisting of: data comprising information regarding the statusof the device; data regarding a blood sample obtained during use of saiddevice; raw data obtained from the processing or the analysis of theblood sample; and analysis results obtained from analysis of raw datafrom the blood sample. 24-27. (canceled)
 28. A system, comprising adevice of claim 1, and further comprising an automated sample collectiondevice configured to receive a blood sample obtained from a puncturewound in said digit.
 29. (canceled)
 30. The system of claim 28, furthercomprising an automated sample analysis device configured to process,analyze, or both, a blood sample obtained from said digit, whereinanalyzing a blood sample comprises detecting a plurality of analytes, ormeasuring the concentrations of a plurality of analytes, in said bloodsample. 31-33. (canceled)
 34. The system of claim 30, further comprisinga communication unit effective to transmit data obtained from said bloodsample.
 35. A method for collecting blood from a digit comprising: atleast partially encircling a human digit with a cuff of a device ofclaim 1; inflating said cuff effective to apply pressure to said digit;lancing said digit effective to puncture the skin of the digit and toallow blood to flow out of the digit; and collecting of at least aportion of said blood flowing out of the digit. 36-39. (canceled) 40.The method of claim 35, wherein said cuff is inflated, and is then atleast partially deflated during collection of at least a portion of saidblood flowing out of the digit.
 41. The method of claim 35, whereininflation of said cuff is inflation to a maximum pressure of about 300millimeters (mm) of mercury (Hg) of pressure. 42-43. (canceled)
 44. Themethod of claim 35, wherein said collecting of at least a portion ofsaid blood flowing out of the digit comprises: beginning the collectionof at least a portion of said blood flowing out of the digit pursuant toa first signal from said device; and ending the collection of bloodflowing out of said digit pursuant to a second signal from said device.45-54. (canceled)
 55. The method of claim 40, wherein said inflatingsaid cuff and then at least partially deflating said cuff comprises aplurality of pulses of cuff inflation.
 56. The method of claim 55,wherein said plurality of pulses of cuff inflation comprises pulsing ata pulse frequency of at least about 15 cycles per minute, where a cycleconsists of an inflation and a deflation of the cuff. 57-60. (canceled)61. The method of claim 35, wherein said digit is disposed within saidcuff and the cuff is inflated for at least about 3 seconds prior tolancing of the digit.
 62. (canceled)
 63. The method of claim 35, whereinsaid digit is disposed within said cuff and the cuff is inflated for atleast about 3 seconds prior to lancing of the digit, the cuff isinflated for about 5 seconds after lancing of the digit, and then aplurality of pulses of cuff inflation are applied to the cuff after saidabout 5 seconds after lancing of the digit. 64-66. (canceled)
 67. Themethod of claim 35, further comprising warming said digit. 68-89.(canceled)